Variant report

Variant	nsv535166
Chromosome Location	chr1:152532577-152555134
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	ATF2	chr1:152549641-152550036	GM12878	blood:	n/a	n/a
2	ATF2	chr1:152537532-152538062	GM12878	blood:	n/a	n/a
3	BATF	chr1:152549573-152550008	GM12878	blood:	n/a	n/a
4	BATF	chr1:152549615-152549949	GM12878	blood:	n/a	n/a
5	BATF	chr1:152537564-152537953	GM12878	blood:	n/a	n/a
6	BATF	chr1:152537583-152537985	GM12878	blood:	n/a	n/a
7	CEBPB	chr1:152535552-152535869	IMR90	lung:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
8	CEBPB	chr1:152535544-152535899	A549	lung:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
9	CEBPB	chr1:152535595-152535869	Hela-S3	cervix:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
10	CEBPB	chr1:152546403-152546497	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr1:152535518-152535885	HepG2	liver:	n/a	chr1:152535674-152535685 chr1:152535692-152535705 chr1:152535673-152535686 chr1:152535693-152535704 chr1:152535806-152535817
12	CTCF	chr1:152552840-152552990	HMEC	breast:	n/a	chr1:152552927-152552936 chr1:152552921-152552939
13	CTCF	chr1:152552800-152552950	NHEK	skin:	n/a	chr1:152552927-152552936 chr1:152552921-152552939
14	CTCF	chr1:152549740-152549890	GM06990	blood:	n/a	n/a
15	CTCF	chr1:152552800-152552950	WERI-Rb-1	eye:	n/a	chr1:152552927-152552936 chr1:152552921-152552939
16	CTCF	chr1:152552201-152552270	MCF-7	breast:	n/a	n/a
17	CTCF	chr1:152538640-152538790	GM12869	blood:	n/a	n/a
18	CTCF	chr1:152544300-152544450	WERI-Rb-1	eye:	n/a	n/a
19	E2F4	chr1:152550054-152550254	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr1:152554133-152554464	MCF10A-Er-Src	breast:	n/a	n/a
21	EBF1	chr1:152551859-152552278	GM12878	blood:	n/a	chr1:152552078-152552089
22	EBF1	chr1:152549703-152549949	GM12878	blood:	n/a	n/a
23	EBF1	chr1:152551863-152552233	GM12878	blood:	n/a	chr1:152552078-152552089
24	EBF1	chr1:152551805-152552302	GM12878	blood:	n/a	chr1:152552078-152552089
25	FOS	chr1:152539192-152539605	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr1:152552901-152553469	MCF10A-Er-Src	breast:	n/a	chr1:152553307-152553315 chr1:152552939-152552947 chr1:152553308-152553315
27	FOS	chr1:152539172-152539644	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr1:152539253-152539483	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr1:152552949-152553402	MCF10A-Er-Src	breast:	n/a	chr1:152553307-152553315 chr1:152553308-152553315
30	FOS	chr1:152552915-152553462	MCF10A-Er-Src	breast:	n/a	chr1:152553307-152553315 chr1:152552939-152552947 chr1:152553308-152553315
31	FOS	chr1:152547010-152547203	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr1:152539193-152539608	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr1:152555026-152555541	MCF10A-Er-Src	breast:	n/a	chr1:152555248-152555258 chr1:152555249-152555256 chr1:152555249-152555257 chr1:152555249-152555257 chr1:152555247-152555259
34	FOS	chr1:152555080-152555419	MCF10A-Er-Src	breast:	n/a	chr1:152555248-152555258 chr1:152555249-152555256 chr1:152555249-152555257 chr1:152555249-152555257 chr1:152555247-152555259
35	FOS	chr1:152547097-152547155	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr1:152554955-152555542	MCF10A-Er-Src	breast:	n/a	chr1:152555248-152555258 chr1:152555249-152555256 chr1:152555249-152555257 chr1:152555249-152555257 chr1:152555247-152555259
37	FOS	chr1:152555036-152555534	MCF10A-Er-Src	breast:	n/a	chr1:152555248-152555258 chr1:152555249-152555256 chr1:152555249-152555257 chr1:152555249-152555257 chr1:152555247-152555259
38	FOS	chr1:152552926-152553507	MCF10A-Er-Src	breast:	n/a	chr1:152553307-152553315 chr1:152552939-152552947 chr1:152553308-152553315
39	IRF3	chr1:152542834-152543044	GM12878	blood:	n/a	n/a
40	IRF4	chr1:152549609-152549966	GM12878	blood:	n/a	n/a
41	IRF4	chr1:152537604-152537978	GM12878	blood:	n/a	n/a
42	IRF4	chr1:152549606-152550028	GM12878	blood:	n/a	n/a
43	JUN	chr1:152553206-152553323	HepG2	liver:	n/a	chr1:152553307-152553315 chr1:152553308-152553315
44	MAFK	chr1:152555095-152555380	K562	blood:	n/a	chr1:152555249-152555259
45	MEF2A	chr1:152537640-152538079	GM12878	blood:	n/a	n/a
46	MYC	chr1:152552943-152553415	MCF10A-Er-Src	breast:	n/a	n/a
47	MYC	chr1:152539283-152539721	MCF10A-Er-Src	breast:	n/a	n/a
48	MYC	chr1:152552931-152553383	MCF10A-Er-Src	breast:	n/a	n/a
49	MYC	chr1:152555068-152555462	MCF10A-Er-Src	breast:	n/a	chr1:152555249-152555258
50	NFIC	chr1:152537468-152537976	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:152552175-152552225	HCPEpiC	choroid plexus:	n/a
2	chr1:152552494-152552544	NHBE	bronchial:	n/a
3	chr1:152552175-152552225	HCPEpiC	choroid plexus:	n/a
4	chr1:152552494-152552544	NHBE	bronchial:	n/a
5	chr1:152538888-152538938	HCF	heart:	n/a
6	chr1:152553244-152553294	HRPEpiC	eye:	n/a
7	chr1:152552175-152552225	PFSK-1	brain:	n/a
8	chr1:152538888-152538938	HRPEpiC	eye:	n/a
9	chr1:152553244-152553294	ovcar-3	ovarian:	n/a
10	chr1:152538888-152538938	NHDF-neo	bronchial:	n/a
11	chr1:152538426-152538476	GM06990	blood:	n/a
12	chr1:152553096-152553146	HUVEC	blood vessel:	n/a
13	chr1:152538888-152538938	HIPEpiC	eye:	n/a
14	chr1:152538426-152538476	HMEC	breast:	n/a
15	chr1:152538857-152538907	ECC-1	luminal epithelium:	n/a
16	chr1:152538426-152538476	PANC-1	pancreas:	n/a
17	chr1:152538888-152538938	AG04449	skin:	fetal
18	chr1:152553096-152553146	PANC-1	pancreas:	n/a
19	chr1:152538426-152538476	U87	brain:	n/a
20	chr1:152538857-152538907	HRCEpiC	kidney:	n/a
21	chr1:152553096-152553146	NB4	blood:	n/a
22	chr1:152538380-152538430	HRPEpiC	eye:	n/a
23	chr1:152538857-152538907	HepG2	liver:	n/a
24	chr1:152553096-152553146	HL-60	blood:	n/a
25	chr1:152552494-152552544	HEEpiC	esophagus:	n/a
26	chr1:152538857-152538907	SAEC	small airway:	n/a
27	chr1:152553096-152553146	CMK	blood:	n/a
28	chr1:152538857-152538907	Jurkat	blood:	n/a
29	chr1:152553244-152553294	SAEC	small airway:	n/a
30	chr1:152552175-152552225	U87	brain:	n/a
31	chr1:152538426-152538476	GM12891	blood:	n/a
32	chr1:152538857-152538907	K562	blood:	n/a
33	chr1:152538426-152538476	AG09309	skin:	n/a
34	chr1:152552494-152552544	GM19239	blood:	n/a
35	chr1:152552175-152552225	SK-N-SH_RA	brain:	n/a
36	chr1:152553096-152553146	SK-N-SH_RA	brain:	n/a
37	chr1:152553244-152553294	AoSMC	blood vessel:	n/a
38	chr1:152538888-152538938	RPTEC	kidney:	n/a
39	chr1:152538426-152538476	HRCEpiC	kidney:	n/a
40	chr1:152553096-152553146	HRCEpiC	kidney:	n/a
41	chr1:152538888-152538938	PANC-1	pancreas:	n/a
42	chr1:152552175-152552225	HRPEpiC	eye:	n/a
43	chr1:152553244-152553294	NHDF-neo	bronchial:	n/a
44	chr1:152552494-152552544	HAEpiC	amniotic membrane:	n/a
45	chr1:152553244-152553294	HepG2	liver:	n/a
46	chr1:152552175-152552225	BE2_C	brain:	n/a
47	chr1:152553096-152553146	HAEpiC	amniotic membrane:	n/a
48	chr1:152552494-152552544	NB4	blood:	n/a
49	chr1:152552175-152552225	A549	lung:	n/a
50	chr1:152553244-152553294	U87	brain:	n/a

Variant related genes	Relation type
LCE3E	TF binding region
LCE3D	TF binding region
LCE3E	CpG island
LCE3D	CpG island

Extended variants
information (count: 787 )
Associated
traits (count: 121 )

Variant overlapped rSNPs/rCNVs (count:787 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73003789	chr1:152534817-152534818	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs112368090	chr1:152534821-152534822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs202236938	chr1:152534827-152534828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560836513	chr1:152534837-152534838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs74363962	chr1:152534842-152534843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs376562213	chr1:152534889-152534890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs562833829	chr1:152534901-152534902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs144473710	chr1:152534909-152534910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs373479375	chr1:152534949-152534950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs4240889	chr1:152534954-152534955	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs4240890	chr1:152535021-152535022	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs79513546	chr1:152535025-152535026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370853710	chr1:152535079-152535080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187165845	chr1:152535085-152535086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192456099	chr1:152535115-152535116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs569217220	chr1:152535170-152535171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs147415449	chr1:152535187-152535188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535881104	chr1:152535204-152535205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549381208	chr1:152535208-152535209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs202031356	chr1:152535226-152535227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200847324	chr1:152535228-152535229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538359787	chr1:152535232-152535233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs139641800	chr1:152535255-152535256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs548419538	chr1:152535256-152535257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs112133766	chr1:152535324-152535325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs578143443	chr1:152535431-152535432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534380694	chr1:152535479-152535480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554201977	chr1:152535496-152535497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574401664	chr1:152535514-152535515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543312517	chr1:152535573-152535574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145168412	chr1:152535576-152535577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs945790	chr1:152535586-152535587	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs534061862	chr1:152535597-152535598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs545214735	chr1:152535626-152535627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs78984538	chr1:152535675-152535676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569161731	chr1:152535679-152535680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547557033	chr1:152535744-152535745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182969838	chr1:152535807-152535808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs372173019	chr1:152535872-152535873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529960120	chr1:152535902-152535903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371345580	chr1:152535918-152535919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74128290	chr1:152535940-152535941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538623249	chr1:152535965-152535966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552013764	chr1:152535973-152535974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565752022	chr1:152535975-152535976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115436389	chr1:152535976-152535977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73003796	chr1:152536027-152536028	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs574236143	chr1:152536128-152536129	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs536952716	chr1:152536135-152536136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556885537	chr1:152536141-152536142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:121)

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
Breast cancer	21611746	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
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152534800-152535000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr1:152535000-152538400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr1:152537400-152537800	Enhancers	GM12878-XiMat	blood
4	chr1:152537800-152538200	Flanking Active TSS	GM12878-XiMat	blood
5	chr1:152538200-152538400	Enhancers	GM12878-XiMat	blood
6	chr1:152538400-152539600	Enhancers	HMEC	breast
7	chr1:152538400-152539800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr1:152538800-152539400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:152538800-152539800	Enhancers	NHEK	skin
10	chr1:152539000-152539600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr1:152539400-152541800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:152541800-152542400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr1:152542000-152544400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr1:152542400-152543000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:152543000-152552600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr1:152546400-152547000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:152547000-152552400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr1:152549400-152549800	Enhancers	GM12878-XiMat	blood
19	chr1:152549400-152550800	Enhancers	Muscle Satellite Cultured Cells	--
20	chr1:152549400-152551400	Enhancers	HSMMtube	muscle
21	chr1:152549400-152551600	Enhancers	HSMM	muscle
22	chr1:152549800-152551400	Weak transcription	GM12878-XiMat	blood
23	chr1:152550800-152555200	Weak transcription	Muscle Satellite Cultured Cells	--
24	chr1:152551400-152552600	Enhancers	GM12878-XiMat	blood
25	chr1:152551600-152552800	Weak transcription	HSMM	muscle
26	chr1:152552400-152553200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr1:152552400-152553400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr1:152552600-152553200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr1:152552600-152553200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr1:152552600-152553400	Enhancers	HMEC	breast
31	chr1:152552800-152553200	Enhancers	HSMM	muscle
32	chr1:152552800-152553400	Enhancers	NHEK	skin
33	chr1:152553400-152555000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr1:152553400-152555000	Weak transcription	HMEC	breast
35	chr1:152553400-152555200	Weak transcription	NHEK	skin
36	chr1:152555000-152555600	Flanking Active TSS	A549	lung
37	chr1:152555000-152555600	Enhancers	HMEC	breast
38	chr1:152555000-152555800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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