Variant report

Variant	esv1818144
Chromosome Location	chr12:11505582-11566327
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	CEBPB	chr12:11550359-11550619	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr12:11550382-11550647	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr12:11538413-11538520	HepG2	liver:	n/a	chr12:11538466-11538477 chr12:11538464-11538475
4	CEBPB	chr12:11514261-11514433	Hela-S3	cervix:	n/a	chr12:11514316-11514325
5	CEBPB	chr12:11538442-11538474	A549	lung:	n/a	n/a
6	CTCF	chr12:11505990-11506144	K562	blood:	n/a	n/a
7	CTCF	chr12:11527332-11527390	GM13976	blood:	n/a	n/a
8	CTCF	chr12:11545730-11545872	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr12:11545750-11545873	GM13977	blood:	n/a	n/a
10	CTCF	chr12:11508581-11508633	GM13976	blood:	n/a	n/a
11	CTCF	chr12:11506052-11506137	MCF-7	breast:	n/a	n/a
12	CTCF	chr12:11528342-11528385	LNCaP	prostate:	n/a	n/a
13	CTCF	chr12:11548021-11548061	LNCaP	prostate:	n/a	n/a
14	CTCF	chr12:11529002-11529034	GM10266	blood:	n/a	n/a
15	CTCF	chr12:11557375-11557427	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr12:11545775-11545832	MCF-7	breast:	n/a	n/a
17	CTCF	chr12:11544846-11544963	GM13976	blood:	n/a	n/a
18	CTCF	chr12:11549867-11549930	GM13976	blood:	n/a	n/a
19	CTCF	chr12:11505592-11505641	GM20000	blood:	n/a	n/a
20	CTCF	chr12:11505978-11506004	Lung_OC	lung:	n/a	n/a
21	CTCF	chr12:11545746-11545856	MCF-7	breast:	n/a	n/a
22	CTCF	chr12:11552280-11552316	GM13977	blood:	n/a	n/a
23	CTCF	chr12:11506036-11506126	MCF-7	breast:	n/a	n/a
24	CTCF	chr12:11548407-11548506	Lung_OC	lung:	n/a	n/a
25	CTCF	chr12:11556054-11556104	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr12:11506136-11506201	GM20000	blood:	n/a	n/a
27	CTCF	chr12:11531414-11531456	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr12:11506021-11506166	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr12:11557353-11557374	Spleen_OC	spleen:	n/a	n/a
30	CTCF	chr12:11545778-11545816	GM12891	blood:	n/a	n/a
31	CTCF	chr12:11545806-11545841	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:11524600-11524750	GM12865	blood:	n/a	n/a
33	CTCF	chr12:11545671-11545700	GM10266	blood:	n/a	n/a
34	CTCF	chr12:11506054-11506114	GM10266	blood:	n/a	n/a
35	E2F4	chr12:11542959-11542990	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr12:11544409-11544699	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr12:11513175-11513539	HUVEC	blood vessel:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360 chr12:11513349-11513360
38	FOS	chr12:11544405-11544693	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr12:11513116-11513579	MCF10A-Er-Src	breast:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360 chr12:11513349-11513360
40	FOS	chr12:11513136-11513561	MCF10A-Er-Src	breast:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360 chr12:11513349-11513360
41	FOS	chr12:11538676-11538692	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr12:11513145-11513524	MCF10A-Er-Src	breast:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360 chr12:11513349-11513360
43	FOS	chr12:11544489-11544699	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr12:11513152-11513541	MCF10A-Er-Src	breast:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360 chr12:11513349-11513360
45	FOSL1	chr12:11513141-11513488	HCT-116	colon:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360
46	FOSL1	chr12:11513158-11513604	HCT-116	colon:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360
47	FOSL2	chr12:11513095-11513514	SK-N-SH	brain:	n/a	chr12:11513350-11513360 chr12:11513351-11513358 chr12:11513350-11513360 chr12:11513351-11513360
48	GABPA	chr12:11546703-11546821	HepG2	liver:	n/a	n/a
49	GABPA	chr12:11546110-11546229	HepG2	liver:	n/a	n/a
50	GABPA	chr12:11545924-11546054	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:11549555-11549605	HPAEpiC	pulmonary alveolar:	n/a
2	chr12:11549555-11549605	HPAEpiC	pulmonary alveolar:	n/a
3	chr12:11548019-11548069	MCF10A-Er-Src	breast:	n/a
4	chr12:11549555-11549605	PrEC	prostate:	n/a
5	chr12:11549192-11549242	K562	blood:	n/a
6	chr12:11508049-11508099	BJ	skin:	n/a
7	chr12:11509583-11509633	AG09309	skin:	n/a
8	chr12:11549192-11549242	PANC-1	pancreas:	n/a
9	chr12:11549192-11549242	U87	brain:	n/a
10	chr12:11508049-11508099	ECC-1	luminal epithelium:	n/a
11	chr12:11548019-11548069	HCF	heart:	n/a
12	chr12:11508049-11508099	HL-60	blood:	n/a
13	chr12:11548867-11548917	SK-N-SH	brain:	n/a
14	chr12:11549555-11549605	NT2-D1	testis:	n/a
15	chr12:11509583-11509633	Hela-S3	cervix:	n/a
16	chr12:11549555-11549605	HCT-116	colon:	n/a
17	chr12:11549192-11549242	H1-hESC	embryonic stem cell:	embryo
18	chr12:11508049-11508099	GM19239	blood:	n/a
19	chr12:11548867-11548917	RPTEC	kidney:	n/a
20	chr12:11508049-11508099	HEEpiC	esophagus:	n/a
21	chr12:11548019-11548069	HCM	heart:	n/a
22	chr12:11548867-11548917	K562	blood:	n/a
23	chr12:11549555-11549605	HUVEC	blood vessel:	n/a
24	chr12:11549192-11549242	HepG2	liver:	n/a
25	chr12:11548019-11548069	U87	brain:	n/a
26	chr12:11549555-11549605	ovcar-3	ovarian:	n/a
27	chr12:11508049-11508099	SK-N-SH	brain:	n/a
28	chr12:11548867-11548917	U87	brain:	n/a
29	chr12:11549192-11549242	AG09309	skin:	n/a
30	chr12:11548019-11548069	MCF-7	breast:	n/a
31	chr12:11508049-11508099	SKMC	muscle:	n/a
32	chr12:11509583-11509633	NB4	blood:	n/a
33	chr12:11508049-11508099	A549	lung:	n/a
34	chr12:11509583-11509633	NH-A	brain:	n/a
35	chr12:11508049-11508099	HMEC	breast:	n/a
36	chr12:11548019-11548069	AG09309	skin:	n/a
37	chr12:11509583-11509633	HCF	heart:	n/a
38	chr12:11548019-11548069	RPTEC	kidney:	n/a
39	chr12:11509583-11509633	HAEpiC	amniotic membrane:	n/a
40	chr12:11509583-11509633	LNCaP	prostate:	n/a
41	chr12:11548867-11548917	HAEpiC	amniotic membrane:	n/a
42	chr12:11549192-11549242	SAEC	small airway:	n/a
43	chr12:11548019-11548069	HAEpiC	amniotic membrane:	n/a
44	chr12:11548019-11548069	CMK	blood:	n/a
45	chr12:11509583-11509633	NT2-D1	testis:	n/a
46	chr12:11549555-11549605	K562	blood:	n/a
47	chr12:11549192-11549242	AG04449	skin:	fetal
48	chr12:11549192-11549242	NT2-D1	testis:	n/a
49	chr12:11509583-11509633	GM06990	blood:	n/a
50	chr12:11548867-11548917	HRE	kidney:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRB1-1	chr12:11554419-11554457	ENSG00000255790.1
2	lnc-PRB1-1	chr12:11552315-11552411	ENSG00000255790.1
3	lnc-PRB1-1	chr12:11559632-11559826	ENSG00000255790.1
4	lnc-PRB1-1	chr12:11552784-11552937	ENSG00000255790.1

Variant related genes	Relation type
PRB2	TF binding region
PRB1	TF binding region
PRB2	CpG island
PRB1	CpG island

Extended variants
information (count: 2476 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2476 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111904312	chr12:11505657-11505658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540041950	chr12:11505836-11505837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200044666	chr12:11505861-11505862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553874165	chr12:11505918-11505919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs573652448	chr12:11505949-11505950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542662358	chr12:11505980-11505981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs374362968	chr12:11506031-11506032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs530189282	chr12:11506044-11506045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs201615726	chr12:11506085-11506086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs199560403	chr12:11506088-11506089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs576051236	chr12:11506094-11506095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201872688	chr12:11506129-11506130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs200283098	chr12:11506141-11506142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs374843401	chr12:11506144-11506145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145243462	chr12:11506157-11506158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533388064	chr12:11506158-11506159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367559123	chr12:11506171-11506172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs78082688	chr12:11506180-11506181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs141582973	chr12:11506183-11506184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199796307	chr12:11506190-11506191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs529377307	chr12:11506196-11506197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371435593	chr12:11506197-11506198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs549421413	chr12:11506210-11506211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs76504934	chr12:11506211-11506212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201751674	chr12:11506213-11506214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs199753072	chr12:11506222-11506223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs368730404	chr12:11506224-11506225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs367909474	chr12:11506244-11506245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139398946	chr12:11506245-11506246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs141114988	chr12:11506259-11506260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs372368931	chr12:11506271-11506272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375239178	chr12:11506275-11506276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs61930108	chr12:11506281-11506282	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201593462	chr12:11506287-11506288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs140825288	chr12:11506288-11506289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs553689169	chr12:11506289-11506290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200893556	chr12:11506297-11506298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201682460	chr12:11506303-11506304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs573740236	chr12:11506316-11506317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201306426	chr12:11506320-11506321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144693892	chr12:11506321-11506322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369194907	chr12:11506334-11506335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575666387	chr12:11506336-11506337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201908587	chr12:11506341-11506342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs544594247	chr12:11506343-11506344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371841290	chr12:11506347-11506348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377208399	chr12:11506350-11506351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200997903	chr12:11506352-11506353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201055825	chr12:11506356-11506357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372966668	chr12:11506364-11506365	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Acute lymphoblastic leukemia	17690704	CNVD
Medulloblastoma	16968546	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Breast cancer	22032731	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	21965145	CNVD
Acute myeloid leukemia	16864856	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Disorders of sex development	21048976	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Prostate cancer	19156837	CNVD
Emphysema	19352772	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Malignant germ cell tumour	17285132	CNVD
Melanoma	18172304	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	21264507	CNVD
Cancer	16751803	CNVD
Testicular cancer	18059402	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Seminomas	18059402	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
Testicular germ cell tumor	18059402	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21858162	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Squamous cell cancer	19607727	CNVD
Prostate cancer	16573809	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16461572	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Acute myeloid leukemia	17237825	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:11505000-11510400	Weak transcription	HUVEC	blood vessel
2	chr12:11506600-11507000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr12:11510000-11511000	Enhancers	Primary neutrophils fromperipheralblood	blood
4	chr12:11510000-11511200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr12:11510400-11511000	Enhancers	HUVEC	blood vessel
6	chr12:11511000-11512400	Weak transcription	HUVEC	blood vessel
7	chr12:11511200-11519600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr12:11512400-11514000	Enhancers	HUVEC	blood vessel
9	chr12:11513000-11513800	Enhancers	HMEC	breast
10	chr12:11513000-11514000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr12:11513000-11514000	Enhancers	NHEK	skin
12	chr12:11513400-11513600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr12:11513600-11514200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr12:11513600-11521200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr12:11516600-11517000	Enhancers	HepG2	liver
16	chr12:11519600-11520200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
17	chr12:11520000-11520600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr12:11520200-11521200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr12:11521200-11521800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr12:11521400-11521600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr12:11529600-11529800	Weak transcription	Primary hematopoietic stem cells	blood
22	chr12:11530200-11531200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr12:11539200-11539400	Flanking Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
24	chr12:11539400-11539800	Enhancers	H9 Cell Line	embryonic stem cell
25	chr12:11544000-11544800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr12:11544000-11544800	Enhancers	HUVEC	blood vessel
27	chr12:11544800-11550000	Weak transcription	HUVEC	blood vessel
28	chr12:11544800-11550200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr12:11550000-11550600	Enhancers	HUVEC	blood vessel
30	chr12:11550000-11550800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr12:11550000-11551000	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr12:11550200-11550800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr12:11550200-11550800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr12:11550200-11551000	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr12:11550800-11551600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr12:11550800-11568400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr12:11551600-11551800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chr12:11560600-11561800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr12:11561000-11561600	Enhancers	HMEC	breast
40	chr12:11561000-11561800	Enhancers	NHEK	skin
41	chr12:11561800-11563000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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