Variant report

Variant	nsv946396
Chromosome Location	chr1:153071819-153088338
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:95)
CpG islands
(count:244)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:95 , 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	chr1:153072809-153073124	MCF-7	breast:	n/a	n/a
6	CEBPB	chr1:153072685-153073167	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr1:153072593-153073269	HCT-116	colon:	n/a	n/a
8	CHD2	chr1:153072795-153073086	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr1:153075162-153075244	LNCaP	prostate:	n/a	n/a
10	CTCF	chr1:153075177-153075215	MCF-7	breast:	n/a	n/a
11	CTCF	chr1:153072114-153072181	LNCaP	prostate:	n/a	n/a
12	CTCF	chr1:153075120-153075270	HEK293	kidney:	n/a	n/a
13	CTCF	chr1:153084680-153084830	MCF-7	breast:	n/a	n/a
14	CTCF	chr1:153075160-153075170	ProgFib	skin:	n/a	n/a
15	CTCF	chr1:153084720-153084870	HEEpiC	esophagus:	n/a	n/a
16	CTCF	chr1:153075210-153075216	A549	lung:	n/a	n/a
17	CTCF	chr1:153075219-153075286	A549	lung:	n/a	n/a
18	CTCF	chr1:153087500-153087650	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr1:153075060-153075210	K562	blood:	n/a	n/a
20	CTCF	chr1:153075100-153075250	WERI-Rb-1	eye:	n/a	n/a
21	E2F4	chr1:153072803-153073112	MCF10A-Er-Src	breast:	n/a	n/a
22	EP300	chr1:153071976-153073524	Hela-S3	cervix:	n/a	n/a
23	EP300	chr1:153087855-153088055	K562	blood:	n/a	n/a
24	FOS	chr1:153072180-153073237	MCF10A-Er-Src	breast:	n/a	chr1:153072839-153072850
25	FOS	chr1:153072269-153073227	MCF10A-Er-Src	breast:	n/a	chr1:153072839-153072850
26	FOS	chr1:153072065-153073279	MCF10A-Er-Src	breast:	n/a	chr1:153072839-153072850
27	FOS	chr1:153072164-153073162	HUVEC	blood vessel:	n/a	chr1:153072839-153072850
28	FOS	chr1:153072067-153073227	MCF10A-Er-Src	breast:	n/a	chr1:153072839-153072850
29	FOSL1	chr1:153072612-153073281	HCT-116	colon:	n/a	n/a
30	FOSL1	chr1:153072022-153073251	HCT-116	colon:	n/a	n/a
31	FOSL2	chr1:153072627-153073022	SK-N-SH	brain:	n/a	n/a
32	FOSL2	chr1:153072722-153073051	MCF-7	breast:	n/a	n/a
33	GABPA	chr1:153085049-153085187	Hela-S3	cervix:	n/a	n/a
34	GATA1	chr1:153087420-153088398	PBDE	blood:	n/a	n/a
35	GATA2	chr1:153087741-153088229	K562	blood:	n/a	n/a
36	GATA2	chr1:153072777-153073165	HUVEC	blood vessel:	n/a	chr1:153072839-153072848 chr1:153073055-153073064
37	GATA2	chr1:153072139-153072461	HUVEC	blood vessel:	n/a	n/a
38	GTF2F1	chr1:153072775-153073077	Hela-S3	cervix:	n/a	n/a
39	JUN	chr1:153072082-153073232	Hela-S3	cervix:	n/a	n/a
40	JUN	chr1:153072330-153072376	HepG2	liver:	n/a	n/a
41	JUND	chr1:153072006-153073254	Hela-S3	cervix:	n/a	n/a
42	JUND	chr1:153072018-153073294	HCT-116	colon:	n/a	n/a
43	JUND	chr1:153072071-153072637	HCT-116	colon:	n/a	n/a
44	JUND	chr1:153087895-153087898	K562	blood:	n/a	n/a
45	JUND	chr1:153072743-153073302	HCT-116	colon:	n/a	n/a
46	MAFF	chr1:153084530-153084625	HepG2	liver:	n/a	n/a
47	MAFK	chr1:153084530-153084666	HepG2	liver:	n/a	chr1:153084545-153084565
48	MAFK	chr1:153072708-153073102	Hela-S3	cervix:	n/a	chr1:153073058-153073067
49	MAFK	chr1:153084480-153084680	HepG2	liver:	n/a	chr1:153084545-153084565
50	MAFK	chr1:153072086-153072355	Hela-S3	cervix:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:153085649-153085699	SKMC	muscle:	n/a
2	chr1:153085998-153086048	HUVEC	blood vessel:	n/a
3	chr1:153085649-153085699	GM12891	blood:	n/a
4	chr1:153085998-153086048	HCPEpiC	choroid plexus:	n/a
5	chr1:153085969-153086019	GM19239	blood:	n/a
6	chr1:153085969-153086019	HCM	heart:	n/a
7	chr1:153085998-153086048	A549	lung:	n/a
8	chr1:153085998-153086048	HRCEpiC	kidney:	n/a
9	chr1:153085998-153086048	HepG2	liver:	n/a
10	chr1:153085649-153085699	MCF-7	breast:	n/a
11	chr1:153085969-153086019	NHDF-neo	bronchial:	n/a
12	chr1:153085998-153086048	HL-60	blood:	n/a
13	chr1:153085649-153085699	AG09319	gingival:	n/a
14	chr1:153085152-153085202	HPAEpiC	pulmonary alveolar:	n/a
15	chr1:153085969-153086019	CMK	blood:	n/a
16	chr1:153085152-153085202	A549	lung:	n/a
17	chr1:153085998-153086048	HCF	heart:	n/a
18	chr1:153085998-153086048	IMR90	lung:	fetal
19	chr1:153085152-153085202	SKMC	muscle:	n/a
20	chr1:153085969-153086019	HCF	heart:	n/a
21	chr1:153085649-153085699	GM12878	blood:	n/a
22	chr1:153085152-153085202	HMEC	breast:	n/a
23	chr1:153085969-153086019	Hela-S3	cervix:	n/a
24	chr1:153085152-153085202	HL-60	blood:	n/a
25	chr1:153085152-153085202	HCM	heart:	n/a
26	chr1:153085969-153086019	AG04449	skin:	fetal
27	chr1:153085998-153086048	MCF-7	breast:	n/a
28	chr1:153085998-153086048	GM19239	blood:	n/a
29	chr1:153085998-153086048	Caco-2	colon:	n/a
30	chr1:153085998-153086048	HEK293	kidney:	embryo
31	chr1:153085649-153085699	AG04450	lung:	fetal
32	chr1:153085649-153085699	HRPEpiC	eye:	n/a
33	chr1:153085969-153086019	ProgFib	skin:	n/a
34	chr1:153085969-153086019	K562	blood:	n/a
35	chr1:153085969-153086019	HL-60	blood:	n/a
36	chr1:153085649-153085699	HL-60	blood:	n/a
37	chr1:153085152-153085202	AG09319	gingival:	n/a
38	chr1:153085649-153085699	SK-N-SH	brain:	n/a
39	chr1:153085998-153086048	HNPCEpiC	eye:	n/a
40	chr1:153085998-153086048	CMK	blood:	n/a
41	chr1:153085152-153085202	GM12892	blood:	n/a
42	chr1:153085998-153086048	HIPEpiC	eye:	n/a
43	chr1:153085152-153085202	U87	brain:	n/a
44	chr1:153085649-153085699	NH-A	brain:	n/a
45	chr1:153085649-153085699	NT2-D1	testis:	n/a
46	chr1:153085969-153086019	GM06990	blood:	n/a
47	chr1:153085649-153085699	SK-N-MC	brain:	n/a
48	chr1:153085152-153085202	AG04450	lung:	fetal
49	chr1:153085152-153085202	ProgFib	skin:	n/a
50	chr1:153085152-153085202	NH-A	brain:	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: 528 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:528 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550913043	chr1:153071833-153071834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1392804	chr1:153071834-153071835	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs79074022	chr1:153071838-153071839	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs11205197	chr1:153071844-153071845	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs143477716	chr1:153071850-153071851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs182811071	chr1:153071854-153071855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547275029	chr1:153071988-153071989	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs12072996	chr1:153071991-153071992	Weak transcription Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs555023619	chr1:153072003-153072004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574928306	chr1:153072005-153072006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543771300	chr1:153072026-153072027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs111932107	chr1:153072070-153072071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs34712959	chr1:153072102-153072103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146740427	chr1:153072137-153072138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs140343397	chr1:153072157-153072158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539246949	chr1:153072180-153072181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs551924384	chr1:153072215-153072216	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs392805	chr1:153072271-153072272	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs528672048	chr1:153072294-153072295	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs112529929	chr1:153072299-153072300	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs74801200	chr1:153072320-153072321	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs562132241	chr1:153072358-153072359	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs530952527	chr1:153072398-153072399	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs187323179	chr1:153072476-153072477	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs145409465	chr1:153072481-153072482	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs191417604	chr1:153072492-153072493	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs546575369	chr1:153072594-153072595	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs566688108	chr1:153072620-153072621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs146458182	chr1:153072626-153072627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs369829286	chr1:153072679-153072680	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs568583446	chr1:153072733-153072734	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537450308	chr1:153072738-153072739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557693326	chr1:153072741-153072742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs182398629	chr1:153072771-153072772	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140761464	chr1:153072793-153072794	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150095231	chr1:153072802-153072803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs547345171	chr1:153072809-153072810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs6587730	chr1:153072875-153072876	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs562169137	chr1:153072932-153072933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372371006	chr1:153072967-153072968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575770504	chr1:153072987-153072988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544710290	chr1:153073020-153073021	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs564552307	chr1:153073040-153073041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187844343	chr1:153073048-153073049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs368820167	chr1:153073071-153073072	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546907931	chr1:153073072-153073073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs79148687	chr1:153073084-153073085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs375133342	chr1:153073091-153073092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537884188	chr1:153073100-153073101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs529074134	chr1:153073115-153073116	Weak transcription Enhancers	n/a	n/a	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:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153067400-153072000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:153070200-153072200	Enhancers	NHEK	skin
3	chr1:153070200-153073600	Enhancers	Hela-S3	cervix
4	chr1:153070800-153072000	Weak transcription	HMEC	breast
5	chr1:153072000-153072600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr1:153072000-153072600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:153072000-153072800	Enhancers	HMEC	breast
8	chr1:153072200-153072600	Flanking Active TSS	NHEK	skin
9	chr1:153072600-153073400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:153072600-153073800	Enhancers	NHEK	skin
11	chr1:153072600-153077600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:153072800-153073400	Weak transcription	HMEC	breast
13	chr1:153073400-153073600	Enhancers	HMEC	breast
14	chr1:153073400-153073800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr1:153075400-153075600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr1:153075600-153075800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr1:153075800-153076000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr1:153077600-153079200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr1:153079200-153080200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:153085000-153086400	Enhancers	Ovary	ovary
21	chr1:153086000-153086200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:153086000-153086400	Enhancers	K562	blood
23	chr1:153086400-153087400	Weak transcription	K562	blood
24	chr1:153086400-153087600	Weak transcription	Ovary	ovary
25	chr1:153087400-153088000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr1:153087400-153088400	Enhancers	K562	blood
27	chr1:153087600-153088000	Enhancers	Ovary	ovary
28	chr1:153087600-153088000	Enhancers	NHEK	skin
29	chr1:153088000-153090200	Weak transcription	Ovary	ovary

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