Variant report

Variant	esv2453475
Chromosome Location	chr13:52803686-52895029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:388)
CpG islands
(count:122)
Chromatin interactive
region (count:4)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr13:52853509-52853730	GM12878	blood:	n/a	chr13:52853641-52853652
2	BATF	chr13:52810391-52810616	GM12878	blood:	n/a	n/a
3	BATF	chr13:52809172-52809423	GM12878	blood:	n/a	n/a
4	CBX3	chr13:52874759-52875007	K562	blood:	n/a	n/a
5	CBX3	chr13:52884093-52884361	K562	blood:	n/a	n/a
6	CBX3	chr13:52884107-52884381	K562	blood:	n/a	n/a
7	CBX3	chr13:52874658-52875125	K562	blood:	n/a	n/a
8	CEBPB	chr13:52864873-52864902	HepG2	liver:	n/a	n/a
9	CEBPB	chr13:52834731-52834822	H1-hESC	embryonic stem cell:	n/a	chr13:52834737-52834748
10	CEBPB	chr13:52834731-52834765	IMR90	lung:	n/a	chr13:52834737-52834748
11	CEBPB	chr13:52834570-52834812	K562	blood:	n/a	chr13:52834737-52834748
12	CEBPB	chr13:52834561-52834763	HepG2	liver:	n/a	chr13:52834737-52834748
13	CEBPD	chr13:52855570-52855946	K562	blood:	n/a	n/a
14	CTCF	chr13:52810520-52810670	AG09309	skin:	n/a	n/a
15	CTCF	chr13:52810401-52810666	A549	lung:	n/a	n/a
16	CTCF	chr13:52810540-52810690	NHEK	skin:	n/a	n/a
17	CTCF	chr13:52882914-52882946	GM10266	blood:	n/a	n/a
18	CTCF	chr13:52810287-52810665	ProgFib	skin:	n/a	n/a
19	CTCF	chr13:52810520-52810670	HEEpiC	esophagus:	n/a	n/a
20	CTCF	chr13:52810431-52810607	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr13:52810520-52810670	HPF	lung:	n/a	n/a
22	CTCF	chr13:52810500-52810650	WERI-Rb-1	eye:	n/a	n/a
23	CTCF	chr13:52810500-52810650	AG04449	skin:	n/a	n/a
24	CTCF	chr13:52867234-52867278	MCF-7	breast:	n/a	n/a
25	CTCF	chr13:52810423-52810675	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr13:52810429-52810646	ECC-1	luminal epithelium:	n/a	n/a
27	CTCF	chr13:52810245-52810251	Gliobla	brain:	n/a	n/a
28	CTCF	chr13:52810140-52810290	AoAF	blood vessel:	n/a	n/a
29	CTCF	chr13:52810500-52810650	GM12873	blood:	n/a	n/a
30	CTCF	chr13:52810500-52810650	GM12866	blood:	n/a	n/a
31	CTCF	chr13:52810321-52810664	Fibrobl	skin:	n/a	n/a
32	CTCF	chr13:52810500-52810650	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr13:52810520-52810670	HEK293	kidney:	n/a	n/a
34	CTCF	chr13:52810500-52810650	AG04450	lung:	n/a	n/a
35	CTCF	chr13:52810500-52810650	HCM	heart:	n/a	n/a
36	CTCF	chr13:52810520-52810670	K562	blood:	n/a	n/a
37	CTCF	chr13:52815600-52815701	Fibrobl	skin:	n/a	n/a
38	CTCF	chr13:52810426-52810854	A549	lung:	n/a	n/a
39	CTCF	chr13:52810157-52810664	A549	lung:	n/a	n/a
40	CTCF	chr13:52810520-52810670	SAEC	small airway:	n/a	n/a
41	CTCF	chr13:52810412-52810665	LNCaP	prostate:	n/a	n/a
42	CTCF	chr13:52810400-52810694	A549	lung:	n/a	n/a
43	CTCF	chr13:52810520-52810670	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr13:52810500-52810650	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr13:52853476-52853565	MCF-7	breast:	n/a	n/a
46	CTCF	chr13:52877285-52877377	MCF-7	breast:	n/a	n/a
47	CTCF	chr13:52810500-52810650	GM12871	blood:	n/a	n/a
48	CTCF	chr13:52810431-52810664	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr13:52810140-52810290	GM12873	blood:	n/a	n/a
50	CTCF	chr13:52810366-52810667	NHEK	skin:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:52866820-52866870	PANC-1	pancreas:	n/a
2	chr13:52886181-52886231	IMR90	lung:	fetal
3	chr13:52866820-52866870	SK-N-SH	brain:	n/a
4	chr13:52886181-52886231	HUVEC	blood vessel:	n/a
5	chr13:52886181-52886231	Hepatocyte	liver:	n/a
6	chr13:52866820-52866870	H1-hESC	embryonic stem cell:	embryo
7	chr13:52886181-52886231	AG10803	skin:	n/a
8	chr13:52886181-52886231	NB4	blood:	n/a
9	chr13:52866820-52866870	HRCEpiC	kidney:	n/a
10	chr13:52866820-52866870	SKMC	muscle:	n/a
11	chr13:52886181-52886231	HCPEpiC	choroid plexus:	n/a
12	chr13:52866820-52866870	SK-N-MC	brain:	n/a
13	chr13:52866820-52866870	MCF-7	breast:	n/a
14	chr13:52886181-52886231	HAEpiC	amniotic membrane:	n/a
15	chr13:52886181-52886231	NHBE	bronchial:	n/a
16	chr13:52866820-52866870	HAEpiC	amniotic membrane:	n/a
17	chr13:52866820-52866870	NT2-D1	testis:	n/a
18	chr13:52866820-52866870	GM12892	blood:	n/a
19	chr13:52886181-52886231	PANC-1	pancreas:	n/a
20	chr13:52866820-52866870	HEEpiC	esophagus:	n/a
21	chr13:52886181-52886231	PFSK-1	brain:	n/a
22	chr13:52866820-52866870	HCM	heart:	n/a
23	chr13:52866820-52866870	HEK293	kidney:	embryo
24	chr13:52886181-52886231	HepG2	liver:	n/a
25	chr13:52866820-52866870	HepG2	liver:	n/a
26	chr13:52886181-52886231	HCM	heart:	n/a
27	chr13:52866820-52866870	MCF10A-Er-Src	breast:	n/a
28	chr13:52866820-52866870	AG10803	skin:	n/a
29	chr13:52866820-52866870	Caco-2	colon:	n/a
30	chr13:52866820-52866870	HUVEC	blood vessel:	n/a
31	chr13:52886181-52886231	NT2-D1	testis:	n/a
32	chr13:52866820-52866870	NH-A	brain:	n/a
33	chr13:52886181-52886231	AG09309	skin:	n/a
34	chr13:52866820-52866870	HCT-116	colon:	n/a
35	chr13:52886181-52886231	A549	lung:	n/a
36	chr13:52866820-52866870	AG09309	skin:	n/a
37	chr13:52866820-52866870	HCF	heart:	n/a
38	chr13:52886181-52886231	ovcar-3	ovarian:	n/a
39	chr13:52866820-52866870	Hepatocyte	liver:	n/a
40	chr13:52886181-52886231	LNCaP	prostate:	n/a
41	chr13:52886181-52886231	HRCEpiC	kidney:	n/a
42	chr13:52886181-52886231	AG04450	lung:	fetal
43	chr13:52886181-52886231	Jurkat	blood:	n/a
44	chr13:52866820-52866870	LNCaP	prostate:	n/a
45	chr13:52886181-52886231	MCF10A-Er-Src	breast:	n/a
46	chr13:52866820-52866870	HRE	kidney:	n/a
47	chr13:52886181-52886231	SK-N-SH_RA	brain:	n/a
48	chr13:52866820-52866870	K562	blood:	n/a
49	chr13:52866820-52866870	AG09319	gingival:	n/a
50	chr13:52866820-52866870	RPTEC	kidney:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:52885798..52888785-chr13:52889900..52891955,2	MCF-7	breast:
2	chr13:52888663..52890246-chr13:52890532..52893511,2	MCF-7	breast:
3	chr13:52888663..52890246-chr13:52890532..52893511,2	MCF-7	breast:
4	chr13:52885798..52888785-chr13:52889900..52891955,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-THSD1-4	chr13:52889589-52890110	NONHSAT033983
2	lnc-THSD1-4	chr13:52890481-52890534	NONHSAT033983
3	lnc-THSD1-4	chr13:52894685-52894718	NONHSAT033983

No data

Variant related genes	Relation type
TPTE2P2	TF binding region
ENSG00000217576	TF binding region
TPTE2P2	CpG island
ENSG00000217576	CpG island

Extended variants
information (count: 701 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150009970	chr13:52809417-52809418	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs544852037	chr13:52809418-52809419	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs555488745	chr13:52809938-52809939	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs575548535	chr13:52810083-52810084	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs537850713	chr13:52810142-52810143	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs57807149	chr13:52810202-52810203	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs114041070	chr13:52810272-52810273	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs540452694	chr13:52810360-52810361	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs560285422	chr13:52810393-52810394	Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs572617905	chr13:52810512-52810513	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs77942724	chr13:52810537-52810538	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs370681465	chr13:52810551-52810552	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs561529000	chr13:52810573-52810574	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs112811658	chr13:52810655-52810656	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs184270740	chr13:52810677-52810678	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs9535928	chr13:52810678-52810679	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs533238011	chr13:52810679-52810680	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs546835713	chr13:52810699-52810700	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs566631145	chr13:52810708-52810709	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs1359791	chr13:52810744-52810745	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs150326359	chr13:52810830-52810831	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs1819307	chr13:52810852-52810853	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs142376312	chr13:52810874-52810875	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs1819308	chr13:52810923-52810924	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs141741256	chr13:52811075-52811076	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs562149828	chr13:52812491-52812492	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs189050123	chr13:52815026-52815027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2768236	chr13:52815081-52815082	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs567513675	chr13:52815109-52815110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530427957	chr13:52815114-52815115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs2760880	chr13:52815158-52815159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181441854	chr13:52815159-52815160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs570323241	chr13:52815198-52815199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539271046	chr13:52815262-52815263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs552782880	chr13:52815311-52815312	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs546981446	chr13:52828587-52828588	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs566800541	chr13:52828605-52828606	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs139094244	chr13:52828614-52828615	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs555674257	chr13:52828616-52828617	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs569185734	chr13:52828617-52828618	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs538074118	chr13:52828621-52828622	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs557900313	chr13:52828622-52828623	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs61433618	chr13:52828630-52828631	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs553026892	chr13:52828697-52828698	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs572788047	chr13:52828705-52828706	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs58345586	chr13:52828706-52828707	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs561990584	chr13:52828741-52828742	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs575974148	chr13:52828743-52828744	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs544434006	chr13:52828744-52828745	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs564085108	chr13:52828745-52828746	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:52810000-52810200	Active TSS	iPS-20b Cell Line	embryonic stem cell
2	chr13:52810000-52810400	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr13:52810000-52810400	Active TSS	H1 Cell Line	embryonic stem cell
4	chr13:52810000-52810400	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr13:52810000-52810400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr13:52810000-52810400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr13:52810000-52810400	Active TSS	Right Atrium	heart
8	chr13:52810200-52810400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
9	chr13:52810200-52810600	Active TSS	HUES64 Cell Line	embryonic stem cell
10	chr13:52810200-52810600	Active TSS	Brain Anterior Caudate	brain
11	chr13:52815000-52815400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr13:52815000-52815400	Enhancers	NHEK	skin
13	chr13:52849200-52849600	Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr13:52849200-52849600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr13:52849200-52849600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr13:52849200-52849600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr13:52849200-52849800	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr13:52849200-52850000	Active TSS	ES-WA7 Cell Line	embryonic stem cell
19	chr13:52849200-52850000	Active TSS	H1 Cell Line	embryonic stem cell
20	chr13:52849200-52850000	Active TSS	H9 Cell Line	embryonic stem cell
21	chr13:52849200-52850000	Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr13:52849200-52850000	Active TSS	HUES6 Cell Line	embryonic stem cell
23	chr13:52849200-52850000	Active TSS	iPS-15b Cell Line	embryonic stem cell
24	chr13:52849200-52850000	Active TSS	iPS-18 Cell Line	embryonic stem cell
25	chr13:52875800-52876000	Enhancers	HSMMtube	muscle
26	chr13:52875800-52876200	Enhancers	HSMM	muscle
27	chr13:52875800-52876600	Enhancers	Muscle Satellite Cultured Cells	--
28	chr13:52875800-52877800	Enhancers	Fetal Muscle Leg	muscle
29	chr13:52876200-52877200	Weak transcription	HSMMtube	muscle
30	chr13:52876200-52877400	Weak transcription	HSMM	muscle
31	chr13:52876600-52877400	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr13:52877200-52877800	Enhancers	HSMMtube	muscle
33	chr13:52877400-52877600	Enhancers	Muscle Satellite Cultured Cells	--
34	chr13:52877400-52877800	Enhancers	HSMM	muscle
35	chr13:52884600-52895400	Weak transcription	K562	blood
36	chr13:52894000-52894400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr13:52894000-52894400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr13:52894000-52894400	Enhancers	HMEC	breast
39	chr13:52894000-52895000	Enhancers	HSMM	muscle
40	chr13:52894200-52894400	Enhancers	Pancreas	Pancrea

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