Variant report

Variant	nsv522439
Chromosome Location	chr12:86020998-86066266
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:337)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:337 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:86036581-86037005	HepG2	liver:	n/a	n/a
2	CEBPB	chr12:86028843-86029069	HepG2	liver:	n/a	n/a
3	CEBPB	chr12:86052168-86052249	K562	blood:	n/a	n/a
4	CEBPB	chr12:86021300-86021775	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr12:86060080-86060137	HepG2	liver:	n/a	n/a
6	CEBPB	chr12:86032813-86033108	HepG2	liver:	n/a	chr12:86033071-86033083
7	CEBPB	chr12:86036541-86036964	HepG2	liver:	n/a	chr12:86036746-86036757
8	CEBPB	chr12:86036576-86036938	A549	lung:	n/a	chr12:86036746-86036757
9	CEBPB	chr12:86036545-86036953	IMR90	lung:	n/a	chr12:86036746-86036757
10	CEBPB	chr12:86036559-86036960	HepG2	liver:	n/a	chr12:86036746-86036757
11	CEBPB	chr12:86036618-86036904	HepG2	liver:	n/a	chr12:86036746-86036757
12	CEBPB	chr12:86052095-86052295	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr12:86036609-86036880	HepG2	liver:	n/a	chr12:86036746-86036757
14	CEBPB	chr12:86027250-86027714	HCT-116	colon:	n/a	n/a
15	CEBPB	chr12:86036533-86037022	MCF-7	breast:	n/a	chr12:86036746-86036757
16	CEBPB	chr12:86019830-86021039	IMR90	lung:	n/a	chr12:86020651-86020662
17	CEBPB	chr12:86036542-86036989	Hela-S3	cervix:	n/a	chr12:86036746-86036757
18	CEBPB	chr12:86036562-86036986	A549	lung:	n/a	chr12:86036746-86036757
19	CEBPB	chr12:86036612-86036933	H1-hESC	embryonic stem cell:	n/a	chr12:86036746-86036757
20	CEBPB	chr12:86036563-86036936	MCF-7	breast:	n/a	chr12:86036746-86036757
21	CEBPB	chr12:86036462-86037083	HCT-116	colon:	n/a	chr12:86036746-86036757
22	CEBPB	chr12:86021336-86021743	IMR90	lung:	n/a	n/a
23	CEBPD	chr12:86036657-86036867	HepG2	liver:	n/a	chr12:86036747-86036758
24	CEBPD	chr12:86036667-86036892	HepG2	liver:	n/a	chr12:86036747-86036758
25	CHD2	chr12:86036616-86036939	HepG2	liver:	n/a	n/a
26	CTCF	chr12:86060590-86060671	GM13976	blood:	n/a	n/a
27	CTCF	chr12:86036740-86036890	Caco-2	colon:	n/a	n/a
28	CTCF	chr12:86036840-86036990	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr12:86036618-86037032	HCT-116	colon:	n/a	n/a
30	CTCF	chr12:86036722-86036916	ProgFib	skin:	n/a	n/a
31	CTCF	chr12:86036717-86036896	Gliobla	brain:	n/a	n/a
32	CTCF	chr12:86024159-86024224	GM10248	blood:	n/a	n/a
33	CTCF	chr12:86036770-86036834	NHEK	skin:	n/a	n/a
34	CTCF	chr12:86036740-86036890	MCF-7	breast:	n/a	n/a
35	CTCF	chr12:86036800-86036950	MCF-7	breast:	n/a	n/a
36	CTCF	chr12:86036625-86037003	IMR90	lung:	n/a	n/a
37	CTCF	chr12:86036720-86036870	Caco-2	colon:	n/a	n/a
38	CTCF	chr12:86036699-86036920	MCF-7	breast:	n/a	n/a
39	CTCF	chr12:86036780-86036930	HEEpiC	esophagus:	n/a	n/a
40	CTCF	chr12:86054788-86054809	GM13976	blood:	n/a	n/a
41	CTCF	chr12:86036760-86036910	RPTEC	kidney:	n/a	n/a
42	CTCF	chr12:86036720-86036870	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr12:86036800-86036950	NHLF	lung:	n/a	n/a
44	CTCF	chr12:86036780-86036930	HMF	breast:	n/a	n/a
45	CTCF	chr12:86036740-86036890	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr12:86036720-86036870	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr12:86036600-86036750	HCM	heart:	n/a	n/a
48	CTCF	chr12:86036740-86036890	GM12865	blood:	n/a	n/a
49	CTCF	chr12:86036776-86036863	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr12:86036733-86036862	SK-N-SH_RA	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:86040467-86040517	NH-A	brain:	n/a
2	chr12:86040467-86040517	T-47D	breast:	n/a
3	chr12:86040467-86040517	ProgFib	skin:	n/a
4	chr12:86040467-86040517	ovcar-3	ovarian:	n/a
5	chr12:86040467-86040517	SK-N-SH_RA	brain:	n/a
6	chr12:86040467-86040517	AoSMC	blood vessel:	n/a
7	chr12:86040467-86040517	SK-N-MC	brain:	n/a
8	chr12:86040467-86040517	HEEpiC	esophagus:	n/a
9	chr12:86040467-86040517	CMK	blood:	n/a
10	chr12:86040467-86040517	Hela-S3	cervix:	n/a
11	chr12:86040467-86040517	MCF-7	breast:	n/a
12	chr12:86040467-86040517	HRE	kidney:	n/a
13	chr12:86040467-86040517	NHBE	bronchial:	n/a
14	chr12:86040467-86040517	ECC-1	luminal epithelium:	n/a
15	chr12:86040467-86040517	HRCEpiC	kidney:	n/a
16	chr12:86040467-86040517	HPAEpiC	pulmonary alveolar:	n/a
17	chr12:86040467-86040517	HUVEC	blood vessel:	n/a
18	chr12:86040467-86040517	A549	lung:	n/a
19	chr12:86040467-86040517	Caco-2	colon:	n/a
20	chr12:86040467-86040517	HCF	heart:	n/a
21	chr12:86040467-86040517	PFSK-1	brain:	n/a
22	chr12:86040467-86040517	GM06990	blood:	n/a
23	chr12:86040467-86040517	HRPEpiC	eye:	n/a
24	chr12:86040467-86040517	Hepatocyte	liver:	n/a
25	chr12:86040467-86040517	LNCaP	prostate:	n/a
26	chr12:86040467-86040517	GM12878	blood:	n/a
27	chr12:86040467-86040517	GM12892	blood:	n/a
28	chr12:86040467-86040517	HAEpiC	amniotic membrane:	n/a
29	chr12:86040467-86040517	SK-N-SH	brain:	n/a
30	chr12:86040467-86040517	GM19239	blood:	n/a
31	chr12:86040467-86040517	H1-hESC	embryonic stem cell:	embryo
32	chr12:86040467-86040517	HEK293	kidney:	embryo
33	chr12:86040467-86040517	AG09309	skin:	n/a
34	chr12:86040467-86040517	NHDF-neo	bronchial:	n/a
35	chr12:86040467-86040517	IMR90	lung:	fetal
36	chr12:86040467-86040517	HepG2	liver:	n/a
37	chr12:86040467-86040517	SAEC	small airway:	n/a
38	chr12:86040467-86040517	HIPEpiC	eye:	n/a
39	chr12:86040467-86040517	RPTEC	kidney:	n/a
40	chr12:86040467-86040517	HCM	heart:	n/a
41	chr12:86040467-86040517	K562	blood:	n/a
42	chr12:86040467-86040517	HL-60	blood:	n/a
43	chr12:86040467-86040517	AG04450	lung:	fetal
44	chr12:86040467-86040517	AG10803	skin:	n/a
45	chr12:86040467-86040517	HCPEpiC	choroid plexus:	n/a
46	chr12:86040467-86040517	U87	brain:	n/a
47	chr12:86040467-86040517	HMEC	breast:	n/a
48	chr12:86040467-86040517	AG04449	skin:	fetal
49	chr12:86040467-86040517	PANC-1	pancreas:	n/a
50	chr12:86040467-86040517	HNPCEpiC	eye:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:86014804..86017595-chr12:86018520..86021053,2	MCF-7	breast:
2	chr12:86031568..86033990-chr12:86035290..86037133,2	K562	blood:
3	chr12:86031568..86033990-chr12:86035290..86037133,2	K562	blood:
4	chr12:86036224..86038282-chr12:86040678..86042966,2	MCF-7	breast:
5	chr12:86039752..86042569-chr12:86049192..86051489,2	MCF-7	breast:
6	chr12:85969213..85970141-chr12:86036344..86037184,4	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000263449	TF binding region
ENSG00000263449	CpG island
ENSG00000263449	chromatin interactions

Extended variants
information (count: 996 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:996 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2199512	chr12:86020998-86020999	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs188553175	chr12:86021019-86021020	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141704124	chr12:86021027-86021028	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191704254	chr12:86021074-86021075	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552428729	chr12:86021209-86021210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs556480815	chr12:86021223-86021224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150530231	chr12:86021281-86021282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545102723	chr12:86021329-86021330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376595576	chr12:86021351-86021352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs570930235	chr12:86021354-86021355	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554123191	chr12:86021376-86021377	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs139937122	chr12:86021379-86021380	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs531994355	chr12:86021448-86021449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561064967	chr12:86021450-86021451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs183207029	chr12:86021474-86021475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141761449	chr12:86021478-86021479	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537803960	chr12:86021490-86021491	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78795197	chr12:86021513-86021514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372905116	chr12:86021529-86021530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs565225315	chr12:86021542-86021543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532412627	chr12:86021552-86021553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188138762	chr12:86021587-86021588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs375840473	chr12:86021591-86021592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6539902	chr12:86021613-86021614	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
25	rs529756656	chr12:86021701-86021702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547842295	chr12:86021808-86021809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs569403128	chr12:86021819-86021820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538097153	chr12:86021830-86021831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552163827	chr12:86021872-86021873	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs571883302	chr12:86021883-86021884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs558904225	chr12:86021946-86021947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs73370478	chr12:86021957-86021958	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs554647748	chr12:86021980-86021981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs191265991	chr12:86022051-86022052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572357548	chr12:86022152-86022153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568734510	chr12:86022196-86022197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs536751351	chr12:86022202-86022203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs555138675	chr12:86022221-86022222	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112738609	chr12:86022244-86022245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376164081	chr12:86022268-86022269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs146234790	chr12:86022343-86022344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565074960	chr12:86022546-86022547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577078295	chr12:86022600-86022601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs7310496	chr12:86022667-86022668	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs559097662	chr12:86022668-86022669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35488196	chr12:86022673-86022674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs186683761	chr12:86022740-86022741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs568512888	chr12:86022746-86022747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192352484	chr12:86022800-86022801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs530509311	chr12:86022868-86022869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

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
Malignant peripheral nerve sheath tumor	18522746	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
Bipolar disorder	19114987	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:86018400-86022000	Enhancers	Hela-S3	cervix
2	chr12:86019000-86022000	Enhancers	HUVEC	blood vessel
3	chr12:86019200-86021200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr12:86019400-86021800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr12:86019600-86021000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr12:86019600-86021400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr12:86019600-86021600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr12:86019600-86021800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr12:86019600-86021800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr12:86019600-86021800	Enhancers	HMEC	breast
11	chr12:86019600-86021800	Enhancers	HSMM	muscle
12	chr12:86019600-86021800	Enhancers	NH-A	brain
13	chr12:86019600-86021800	Enhancers	NHDF-Ad	bronchial
14	chr12:86019600-86021800	Enhancers	NHLF	lung
15	chr12:86019600-86022000	Enhancers	Osteobl	bone
16	chr12:86019800-86021200	Enhancers	Primary hematopoietic stem cells	blood
17	chr12:86019800-86021600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr12:86019800-86021800	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr12:86020200-86021600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr12:86020400-86021000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr12:86020400-86021800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr12:86020400-86021800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr12:86020600-86022000	Enhancers	Muscle Satellite Cultured Cells	--
24	chr12:86020800-86022000	Enhancers	NHEK	skin
25	chr12:86021000-86024000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr12:86021600-86024400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr12:86021600-86026200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr12:86021800-86025800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr12:86021800-86025800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr12:86021800-86026000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr12:86021800-86027200	Weak transcription	NHDF-Ad	bronchial
32	chr12:86022000-86024400	Weak transcription	Osteobl	bone
33	chr12:86022000-86024600	Weak transcription	NHEK	skin
34	chr12:86022000-86026000	Weak transcription	Hela-S3	cervix
35	chr12:86022000-86026000	Weak transcription	HUVEC	blood vessel
36	chr12:86024000-86024800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr12:86024400-86024600	Enhancers	Osteobl	bone
38	chr12:86024400-86025000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr12:86024600-86026600	Enhancers	NHEK	skin
40	chr12:86024800-86026000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr12:86025000-86026000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
42	chr12:86025800-86026400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr12:86025800-86026600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr12:86026000-86026200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr12:86026000-86026400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr12:86026000-86026400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr12:86026000-86026600	Enhancers	HUVEC	blood vessel
48	chr12:86026000-86027400	Enhancers	Hela-S3	cervix
49	chr12:86026200-86026400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr12:86026400-86027200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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