Variant report

Variant	esv18497
Chromosome Location	chr1:153069195-153087963
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:97)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:97 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr1:153072106-153072249	Hela-S3	cervix:	n/a	n/a
2	CBX3	chr1:153072732-153073222	HCT-116	colon:	n/a	n/a
3	CEBPB	chr1:153072025-153072481	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr1:153072214-153073260	HCT-116	colon:	n/a	n/a
5	CEBPB	chr1:153070459-153070753	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr1:153072593-153073269	HCT-116	colon:	n/a	n/a
7	CEBPB	chr1:153072809-153073124	MCF-7	breast:	n/a	n/a
8	CEBPB	chr1:153072685-153073167	Hela-S3	cervix:	n/a	n/a
9	CHD2	chr1:153072795-153073086	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr1:153075160-153075170	ProgFib	skin:	n/a	n/a
11	CTCF	chr1:153075060-153075210	K562	blood:	n/a	n/a
12	CTCF	chr1:153075120-153075270	HEK293	kidney:	n/a	n/a
13	CTCF	chr1:153072114-153072181	LNCaP	prostate:	n/a	n/a
14	CTCF	chr1:153075210-153075216	A549	lung:	n/a	n/a
15	CTCF	chr1:153075219-153075286	A549	lung:	n/a	n/a
16	CTCF	chr1:153084720-153084870	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr1:153075100-153075250	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr1:153075177-153075215	MCF-7	breast:	n/a	n/a
19	CTCF	chr1:153087500-153087650	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr1:153084680-153084830	MCF-7	breast:	n/a	n/a
21	CTCF	chr1:153075162-153075244	LNCaP	prostate:	n/a	n/a
22	E2F4	chr1:153072803-153073112	MCF10A-Er-Src	breast:	n/a	n/a
23	EP300	chr1:153087855-153088055	K562	blood:	n/a	n/a
24	EP300	chr1:153070217-153070881	Hela-S3	cervix:	n/a	chr1:153070612-153070626
25	EP300	chr1:153071976-153073524	Hela-S3	cervix:	n/a	n/a
26	FOS	chr1:153072180-153073237	MCF10A-Er-Src	breast:	n/a	chr1:153072839-153072850
27	FOS	chr1:153072065-153073279	MCF10A-Er-Src	breast:	n/a	chr1:153072839-153072850
28	FOS	chr1:153072067-153073227	MCF10A-Er-Src	breast:	n/a	chr1:153072839-153072850
29	FOS	chr1:153072164-153073162	HUVEC	blood vessel:	n/a	chr1:153072839-153072850
30	FOS	chr1:153072269-153073227	MCF10A-Er-Src	breast:	n/a	chr1:153072839-153072850
31	FOSL1	chr1:153072612-153073281	HCT-116	colon:	n/a	n/a
32	FOSL1	chr1:153072022-153073251	HCT-116	colon:	n/a	n/a
33	FOSL2	chr1:153072722-153073051	MCF-7	breast:	n/a	n/a
34	FOSL2	chr1:153072627-153073022	SK-N-SH	brain:	n/a	n/a
35	GABPA	chr1:153085049-153085187	Hela-S3	cervix:	n/a	n/a
36	GATA1	chr1:153068392-153069584	PBDE	blood:	n/a	chr1:153069330-153069340 chr1:153069182-153069192
37	GATA1	chr1:153087420-153088398	PBDE	blood:	n/a	n/a
38	GATA2	chr1:153087741-153088229	K562	blood:	n/a	n/a
39	GATA2	chr1:153072777-153073165	HUVEC	blood vessel:	n/a	chr1:153072839-153072848 chr1:153073055-153073064
40	GATA2	chr1:153072139-153072461	HUVEC	blood vessel:	n/a	n/a
41	GTF2F1	chr1:153072775-153073077	Hela-S3	cervix:	n/a	n/a
42	JUN	chr1:153072082-153073232	Hela-S3	cervix:	n/a	n/a
43	JUN	chr1:153072330-153072376	HepG2	liver:	n/a	n/a
44	JUND	chr1:153072743-153073302	HCT-116	colon:	n/a	n/a
45	JUND	chr1:153072006-153073254	Hela-S3	cervix:	n/a	n/a
46	JUND	chr1:153072018-153073294	HCT-116	colon:	n/a	n/a
47	JUND	chr1:153072071-153072637	HCT-116	colon:	n/a	n/a
48	JUND	chr1:153087895-153087898	K562	blood:	n/a	n/a
49	MAFF	chr1:153084530-153084625	HepG2	liver:	n/a	n/a
50	MAFK	chr1:153084480-153084680	HepG2	liver:	n/a	chr1:153084545-153084565

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153085998-153086048	AG04450	lung:	fetal
2	chr1:153085649-153085699	MCF10A-Er-Src	breast:	n/a
3	chr1:153085998-153086048	BJ	skin:	n/a
4	chr1:153085998-153086048	GM12891	blood:	n/a
5	chr1:153085649-153085699	NH-A	brain:	n/a
6	chr1:153085969-153086019	NT2-D1	testis:	n/a
7	chr1:153085998-153086048	GM12892	blood:	n/a
8	chr1:153085969-153086019	SK-N-SH_RA	brain:	n/a
9	chr1:153085998-153086048	HCM	heart:	n/a
10	chr1:153085649-153085699	ECC-1	luminal epithelium:	n/a
11	chr1:153085649-153085699	SK-N-SH_RA	brain:	n/a
12	chr1:153085649-153085699	HPAEpiC	pulmonary alveolar:	n/a
13	chr1:153085998-153086048	ECC-1	luminal epithelium:	n/a
14	chr1:153085969-153086019	GM12878	blood:	n/a
15	chr1:153085649-153085699	Jurkat	blood:	n/a
16	chr1:153085152-153085202	RPTEC	kidney:	n/a
17	chr1:153085649-153085699	SAEC	small airway:	n/a
18	chr1:153085998-153086048	HAEpiC	amniotic membrane:	n/a
19	chr1:153085152-153085202	T-47D	breast:	n/a
20	chr1:153085969-153086019	PANC-1	pancreas:	n/a
21	chr1:153085969-153086019	U87	brain:	n/a
22	chr1:153085649-153085699	U87	brain:	n/a
23	chr1:153085969-153086019	PrEC	prostate:	n/a
24	chr1:153085152-153085202	HRPEpiC	eye:	n/a
25	chr1:153085152-153085202	GM19239	blood:	n/a
26	chr1:153085152-153085202	SK-N-MC	brain:	n/a
27	chr1:153085969-153086019	GM19239	blood:	n/a
28	chr1:153085998-153086048	HPAEpiC	pulmonary alveolar:	n/a
29	chr1:153085649-153085699	IMR90	lung:	fetal
30	chr1:153085649-153085699	GM06990	blood:	n/a
31	chr1:153085152-153085202	ECC-1	luminal epithelium:	n/a
32	chr1:153085152-153085202	ProgFib	skin:	n/a
33	chr1:153085998-153086048	MCF-7	breast:	n/a
34	chr1:153085969-153086019	HUVEC	blood vessel:	n/a
35	chr1:153085998-153086048	AG10803	skin:	n/a
36	chr1:153085152-153085202	GM12892	blood:	n/a
37	chr1:153085969-153086019	HIPEpiC	eye:	n/a
38	chr1:153085998-153086048	PFSK-1	brain:	n/a
39	chr1:153085998-153086048	Jurkat	blood:	n/a
40	chr1:153085152-153085202	HIPEpiC	eye:	n/a
41	chr1:153085998-153086048	GM19239	blood:	n/a
42	chr1:153085969-153086019	ProgFib	skin:	n/a
43	chr1:153085152-153085202	HepG2	liver:	n/a
44	chr1:153085649-153085699	HEEpiC	esophagus:	n/a
45	chr1:153085649-153085699	RPTEC	kidney:	n/a
46	chr1:153085649-153085699	NHDF-neo	bronchial:	n/a
47	chr1:153085649-153085699	HRCEpiC	kidney:	n/a
48	chr1:153085152-153085202	A549	lung:	n/a
49	chr1:153085152-153085202	BE2_C	brain:	n/a
50	chr1:153085998-153086048	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:153066495..153069197-chr1:153073553..153075701,2	K562	blood:
2	chr1:153086209..153088647-chr1:153089320..153091909,2	K562	blood:

No data

Variant related genes	Relation type
SPRR2F	TF binding region
SPRR2E	TF binding region
SPRR2F	CpG island
SPRR2E	CpG island
ENSG00000203785	chromatin interactions

Extended variants
information (count: 615 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:615 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560972491	chr1:153069208-153069209	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs529906333	chr1:153069234-153069235	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs189638389	chr1:153069238-153069239	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs143853807	chr1:153069282-153069283	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs148382029	chr1:153069294-153069295	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs551854509	chr1:153069317-153069318	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs114462629	chr1:153069340-153069341	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs74133276	chr1:153069342-153069343	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs560352743	chr1:153069400-153069401	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs71769658	chr1:153069406-153069407	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs11581933	chr1:153069407-153069408	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs114520305	chr1:153069430-153069431	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs536436281	chr1:153069431-153069432	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs114302687	chr1:153069462-153069463	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs185315716	chr1:153069466-153069467	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs538652183	chr1:153069482-153069483	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs141129286	chr1:153069534-153069535	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs11205195	chr1:153069584-153069585	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs558639984	chr1:153069593-153069594	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs572395640	chr1:153069595-153069596	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs35114774	chr1:153069625-153069626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs149619711	chr1:153069653-153069654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200092329	chr1:153069656-153069657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs34048517	chr1:153069662-153069663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534657637	chr1:153069686-153069687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs77592975	chr1:153069690-153069691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs141564326	chr1:153069876-153069877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs543607287	chr1:153069888-153069889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs563392741	chr1:153069969-153069970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs576964292	chr1:153069979-153069980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs61811907	chr1:153070024-153070025	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs190308869	chr1:153070070-153070071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528069652	chr1:153070083-153070084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs140070830	chr1:153070131-153070132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs529331865	chr1:153070143-153070144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145495465	chr1:153070154-153070155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530254774	chr1:153070163-153070164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181183920	chr1:153070225-153070226	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs569826108	chr1:153070270-153070271	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs569106094	chr1:153070380-153070381	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs552638143	chr1:153070524-153070525	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs199619030	chr1:153070548-153070549	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs535332959	chr1:153070561-153070562	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs565968614	chr1:153070567-153070568	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs535001619	chr1:153070645-153070646	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs61811908	chr1:153070662-153070663	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs111283376	chr1:153070668-153070669	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs186588698	chr1:153070708-153070709	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs557150754	chr1:153070758-153070759	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs189670388	chr1:153070789-153070790	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153067400-153070200	Weak transcription	NHEK	skin
2	chr1:153067400-153072000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr1:153068200-153069600	Enhancers	K562	blood
4	chr1:153068400-153069200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr1:153068400-153069200	Enhancers	Hela-S3	cervix
6	chr1:153069200-153070200	Weak transcription	Hela-S3	cervix
7	chr1:153070200-153072200	Enhancers	NHEK	skin
8	chr1:153070200-153073600	Enhancers	Hela-S3	cervix
9	chr1:153070400-153070600	Enhancers	HMEC	breast
10	chr1:153070800-153072000	Weak transcription	HMEC	breast
11	chr1:153072000-153072600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:153072000-153072600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:153072000-153072800	Enhancers	HMEC	breast
14	chr1:153072200-153072600	Flanking Active TSS	NHEK	skin
15	chr1:153072600-153073400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr1:153072600-153073800	Enhancers	NHEK	skin
17	chr1:153072600-153077600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr1:153072800-153073400	Weak transcription	HMEC	breast
19	chr1:153073400-153073600	Enhancers	HMEC	breast
20	chr1:153073400-153073800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr1:153075400-153075600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr1:153075600-153075800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr1:153075800-153076000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr1:153077600-153079200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr1:153079200-153080200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:153085000-153086400	Enhancers	Ovary	ovary
27	chr1:153086000-153086200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr1:153086000-153086400	Enhancers	K562	blood
29	chr1:153086400-153087400	Weak transcription	K562	blood
30	chr1:153086400-153087600	Weak transcription	Ovary	ovary
31	chr1:153087400-153088000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr1:153087400-153088400	Enhancers	K562	blood
33	chr1:153087600-153088000	Enhancers	Ovary	ovary
34	chr1:153087600-153088000	Enhancers	NHEK	skin

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