Variant report

Variant	nsv900261
Chromosome Location	chr13:63179285-63553876
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:874)
CpG islands
(count:61)
Chromatin interactive
region (count:2)
LncRNA
region (count:32)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:63216982-63217579	GM12878	blood:	n/a	n/a
2	ATF2	chr13:63217071-63217515	GM12878	blood:	n/a	n/a
3	ATF3	chr13:63216965-63217632	HCT-116	colon:	n/a	n/a
4	ATF3	chr13:63217044-63217471	A549	lung:	n/a	n/a
5	ATF3	chr13:63217000-63217643	HCT-116	colon:	n/a	n/a
6	BACH1	chr13:63295336-63295437	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr13:63217072-63217610	GM12878	blood:	n/a	chr13:63217373-63217384 chr13:63217318-63217329 chr13:63217301-63217312 chr13:63217346-63217357
8	BATF	chr13:63217055-63217560	GM12878	blood:	n/a	chr13:63217373-63217384 chr13:63217318-63217329 chr13:63217301-63217312 chr13:63217346-63217357
9	BATF	chr13:63449339-63449575	GM12878	blood:	n/a	chr13:63449426-63449437
10	BATF	chr13:63218039-63218384	GM12878	blood:	n/a	n/a
11	BCL11A	chr13:63217076-63217531	GM12878	blood:	n/a	n/a
12	BCL11A	chr13:63217051-63217596	GM12878	blood:	n/a	n/a
13	BCL3	chr13:63217091-63217547	GM12878	blood:	n/a	n/a
14	BCL3	chr13:63217072-63217587	GM12878	blood:	n/a	n/a
15	BHLHE40	chr13:63321881-63322081	HepG2	liver:	n/a	n/a
16	BHLHE40	chr13:63269331-63269362	GM12878	blood:	n/a	n/a
17	BRCA1	chr13:63488576-63488593	GM12878	blood:	n/a	n/a
18	CBX3	chr13:63216909-63217794	HCT-116	colon:	n/a	n/a
19	CBX3	chr13:63280130-63280699	HCT-116	colon:	n/a	n/a
20	CBX3	chr13:63216921-63217854	HCT-116	colon:	n/a	n/a
21	CEBPB	chr13:63432076-63432444	Hela-S3	cervix:	n/a	chr13:63432246-63432257
22	CEBPB	chr13:63345122-63345399	IMR90	lung:	n/a	chr13:63345274-63345285
23	CEBPB	chr13:63227463-63227779	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr13:63411996-63412388	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr13:63396473-63396780	HepG2	liver:	n/a	chr13:63396623-63396634 chr13:63396594-63396605 chr13:63396592-63396603 chr13:63396625-63396636 chr13:63396625-63396634 chr13:63396589-63396606
26	CEBPB	chr13:63322272-63322576	HepG2	liver:	n/a	chr13:63322373-63322382 chr13:63322371-63322382
27	CEBPB	chr13:63497473-63497639	HepG2	liver:	n/a	chr13:63497538-63497549 chr13:63497537-63497550 chr13:63497626-63497637
28	CEBPB	chr13:63412008-63412411	IMR90	lung:	n/a	n/a
29	CEBPB	chr13:63209283-63209707	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr13:63458384-63458584	HepG2	liver:	n/a	chr13:63458505-63458516 chr13:63458505-63458518 chr13:63458505-63458518
31	CEBPB	chr13:63345100-63345369	A549	lung:	n/a	chr13:63345274-63345285
32	CEBPB	chr13:63188505-63188772	A549	lung:	n/a	chr13:63188664-63188675 chr13:63188664-63188677
33	CEBPB	chr13:63293850-63294143	IMR90	lung:	n/a	n/a
34	CEBPB	chr13:63345104-63345397	HepG2	liver:	n/a	chr13:63345274-63345285
35	CEBPB	chr13:63217074-63217543	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr13:63507671-63507971	IMR90	lung:	n/a	n/a
37	CEBPB	chr13:63322255-63322610	IMR90	lung:	n/a	chr13:63322373-63322382 chr13:63322371-63322382
38	CEBPB	chr13:63432074-63432428	HepG2	liver:	n/a	chr13:63432246-63432257
39	CEBPB	chr13:63420304-63420618	IMR90	lung:	n/a	chr13:63420421-63420434
40	CEBPB	chr13:63378022-63378232	HepG2	liver:	n/a	chr13:63378135-63378148 chr13:63378136-63378147 chr13:63378134-63378151 chr13:63378135-63378148
41	CEBPB	chr13:63217091-63217597	GM12878	blood:	n/a	n/a
42	CEBPB	chr13:63217090-63217454	A549	lung:	n/a	n/a
43	CEBPB	chr13:63188506-63188807	HepG2	liver:	n/a	chr13:63188664-63188675 chr13:63188664-63188677
44	CEBPB	chr13:63342444-63342551	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr13:63345098-63345406	Hela-S3	cervix:	n/a	chr13:63345274-63345285
46	CEBPB	chr13:63506091-63506628	IMR90	lung:	n/a	n/a
47	CEBPB	chr13:63432074-63432425	IMR90	lung:	n/a	chr13:63432246-63432257
48	CEBPB	chr13:63432068-63432403	A549	lung:	n/a	chr13:63432246-63432257
49	CEBPB	chr13:63284596-63284820	HepG2	liver:	n/a	chr13:63284686-63284697 chr13:63284686-63284699 chr13:63284683-63284700
50	CEBPB	chr13:63217013-63217667	HCT-116	colon:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:63264349-63264399	HAEpiC	amniotic membrane:	n/a
2	chr13:63264349-63264399	BE2_C	brain:	n/a
3	chr13:63264349-63264399	GM19239	blood:	n/a
4	chr13:63264349-63264399	PFSK-1	brain:	n/a
5	chr13:63264349-63264399	HCM	heart:	n/a
6	chr13:63264349-63264399	AG09309	skin:	n/a
7	chr13:63264349-63264399	AG09319	gingival:	n/a
8	chr13:63264349-63264399	HCPEpiC	choroid plexus:	n/a
9	chr13:63264349-63264399	HRE	kidney:	n/a
10	chr13:63264349-63264399	GM12878	blood:	n/a
11	chr13:63264349-63264399	NH-A	brain:	n/a
12	chr13:63264349-63264399	MCF-7	breast:	n/a
13	chr13:63264349-63264399	AG10803	skin:	n/a
14	chr13:63264349-63264399	HNPCEpiC	eye:	n/a
15	chr13:63264349-63264399	HCT-116	colon:	n/a
16	chr13:63264349-63264399	HepG2	liver:	n/a
17	chr13:63264349-63264399	Jurkat	blood:	n/a
18	chr13:63264349-63264399	NHDF-neo	bronchial:	n/a
19	chr13:63264349-63264399	MCF10A-Er-Src	breast:	n/a
20	chr13:63264349-63264399	ovcar-3	ovarian:	n/a
21	chr13:63264349-63264399	CMK	blood:	n/a
22	chr13:63264349-63264399	NHBE	bronchial:	n/a
23	chr13:63264349-63264399	ECC-1	luminal epithelium:	n/a
24	chr13:63264349-63264399	HIPEpiC	eye:	n/a
25	chr13:63264349-63264399	AoSMC	blood vessel:	n/a
26	chr13:63264349-63264399	H1-hESC	embryonic stem cell:	embryo
27	chr13:63264349-63264399	HUVEC	blood vessel:	n/a
28	chr13:63264349-63264399	NT2-D1	testis:	n/a
29	chr13:63264349-63264399	GM12892	blood:	n/a
30	chr13:63264349-63264399	K562	blood:	n/a
31	chr13:63264349-63264399	PANC-1	pancreas:	n/a
32	chr13:63264349-63264399	PrEC	prostate:	n/a
33	chr13:63264349-63264399	BJ	skin:	n/a
34	chr13:63264349-63264399	GM06990	blood:	n/a
35	chr13:63264349-63264399	ProgFib	skin:	n/a
36	chr13:63264349-63264399	AG04449	skin:	fetal
37	chr13:63264349-63264399	HEK293	kidney:	embryo
38	chr13:63264349-63264399	SK-N-MC	brain:	n/a
39	chr13:63264349-63264399	U87	brain:	n/a
40	chr13:63264349-63264399	HPAEpiC	pulmonary alveolar:	n/a
41	chr13:63264349-63264399	HEEpiC	esophagus:	n/a
42	chr13:63264349-63264399	HCF	heart:	n/a
43	chr13:63264349-63264399	HL-60	blood:	n/a
44	chr13:63264349-63264399	SK-N-SH	brain:	n/a
45	chr13:63264349-63264399	HRCEpiC	kidney:	n/a
46	chr13:63264349-63264399	HRPEpiC	eye:	n/a
47	chr13:63264349-63264399	GM12891	blood:	n/a
48	chr13:63264349-63264399	SK-N-SH_RA	brain:	n/a
49	chr13:63264349-63264399	HMEC	breast:	n/a
50	chr13:63264349-63264399	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:97173416..97174286-chr13:63349578..63350296,2	MCF-7	breast:
2	chr13:63305859..63307828-chr13:63368512..63371200,2	K562	blood:

(count:32 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH20-3	chr13:63305993-63306328	ENSG00000228669
2	lnc-PCDH20-18	chr13:63300903-63301293	NONHSAT034152
3	lnc-PCDH20-20	chr13:63547376-63548145	NONHSAT034156
4	lnc-PCDH20-18	chr13:63311883-63313757	ucscGeneNc_uc010aeh_1
5	lnc-PCDH20-3	chr13:63306227-63306313	ENSG00000228669
6	lnc-PCDH20-17	chr13:63186486-63186509	NONHSAT034147
7	lnc-PCDH20-18	chr13:63315448-63316259	ucscGeneNc_uc010aeh_1
8	lnc-AL445989.1-23	chr13:63220133-63220531	NONHSAT034150
9	lnc-PCDH20-4	chr13:63321841-63322054	NONHSAT034155
10	lnc-PCDH20-3	chr13:63246418-63246591	ENSG00000228669
11	lnc-PCDH20-3	chr13:63260138-63260227	ENSG00000228669
12	lnc-PCDH20-4	chr13:63321740-63322054	XLOC_010638
13	lnc-PCDH20-17	chr13:63201523-63201643	NONHSAT034148
14	lnc-PCDH20-18	chr13:63300981-63301286	ucscGeneNc_uc010aeh_1
15	lnc-PCDH20-20	chr13:63462230-63462334	NONHSAT034156
16	lnc-PCDH20-3	chr13:63274749-63274830	ENSG00000228669
17	lnc-PCDH20-20	chr13:63475482-63475599	NONHSAT034156
18	lnc-PCDH20-4	chr13:63370693-63370823	XLOC_010638
19	lnc-PCDH20-17	chr13:63199185-63199216	NONHSAT034148
20	lnc-PCDH20-4	chr13:63368629-63368706	NONHSAT034155
21	lnc-PCDH20-20	chr13:63474519-63474543	NONHSAT034156
22	lnc-PCDH20-18	chr13:63303588-63303986	NONHSAT034152
23	lnc-PCDH20-17	chr13:63189084-63189152	NONHSAT034147
24	lnc-PCDH20-17	chr13:63189084-63189137	l_864_chr13:63139750-63189137_testes
25	lnc-PCDH20-4	chr13:63368629-63368704	XLOC_010638
26	lnc-PCDH20-20	chr13:63506481-63506671	NONHSAT034156
27	lnc-PCDH20-18	chr13:63303588-63303661	ucscGeneNc_uc010aeh_1
28	lnc-PCDH20-20	chr13:63458505-63459173	NONHSAT034156
29	lnc-PCDH20-18	chr13:63311204-63311359	ucscGeneNc_uc010aeh_1
30	lnc-PCDH20-17	chr13:63210043-63210152	NONHSAT034148
31	lnc-AL445989.1-23	chr13:63222838-63223214	NONHSAT034150
32	lnc-PCDH20-3	chr13:63306427-63306492	ENSG00000228669

No data

Variant related genes	Relation type
LINC00448	TF binding region
LINC00448	CpG island
ENSG00000095637	chromatin interactions
ENSG00000228669	chromatin interactions

Extended variants
information (count: 3541 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:3541 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115214064	chr13:63186021-63186022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530405563	chr13:63186023-63186024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542308683	chr13:63186035-63186036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs374630585	chr13:63186063-63186064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371979934	chr13:63186067-63186068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181655901	chr13:63186071-63186072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185775779	chr13:63186080-63186081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs571430373	chr13:63186097-63186098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs148418473	chr13:63186126-63186127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs551882512	chr13:63186146-63186147	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs192031031	chr13:63186147-63186148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs537433233	chr13:63186152-63186153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9528541	chr13:63186156-63186157	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs567654959	chr13:63186157-63186158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs193110786	chr13:63187685-63187686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185513960	chr13:63187694-63187695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556885681	chr13:63187712-63187713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs150508434	chr13:63187737-63187738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573593131	chr13:63187742-63187743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs111617971	chr13:63187767-63187768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs74082986	chr13:63187800-63187801	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs139826583	chr13:63187809-63187810	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs546633399	chr13:63187855-63187856	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs190373218	chr13:63187873-63187874	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs199527203	chr13:63187966-63187967	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs538915030	chr13:63188057-63188058	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs143883093	chr13:63188113-63188114	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs542451177	chr13:63188154-63188155	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs1909488	chr13:63188177-63188178	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs60156646	chr13:63188254-63188255	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs191444257	chr13:63188258-63188259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs533659406	chr13:63188262-63188263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146867162	chr13:63188281-63188282	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs576936768	chr13:63188285-63188286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs562324111	chr13:63188289-63188290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs183579606	chr13:63188328-63188329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs140727655	chr13:63188340-63188341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs368971539	chr13:63188351-63188352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs150024256	chr13:63188352-63188353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs7338526	chr13:63188365-63188366	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs145359464	chr13:63188472-63188473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564907538	chr13:63188492-63188493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527239769	chr13:63188517-63188518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540335006	chr13:63188530-63188531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs79885142	chr13:63188646-63188647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7321983	chr13:63188750-63188751	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs550838930	chr13:63188766-63188767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565063496	chr13:63189088-63189089	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs75044362	chr13:63189128-63189129	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs376378847	chr13:63189136-63189137	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:102)

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
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	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
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Anaplastic thyroid cancer	18753363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	21346763	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Autism	20531469	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:156 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:63186000-63186200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:63187600-63187800	Enhancers	Fetal Heart	heart
3	chr13:63187800-63188200	Flanking Active TSS	Fetal Heart	heart
4	chr13:63188000-63188400	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr13:63188000-63188400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr13:63188000-63188400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr13:63188200-63188800	Enhancers	Fetal Heart	heart
8	chr13:63196000-63196800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr13:63199600-63201400	Active TSS	HSMMtube	muscle
10	chr13:63199800-63200400	ZNF genes & repeats	Fetal Muscle Trunk	muscle
11	chr13:63200400-63201200	ZNF genes & repeats	Fetal Muscle Leg	muscle
12	chr13:63200400-63202000	Active TSS	Fetal Muscle Trunk	muscle
13	chr13:63201200-63201600	Active TSS	Fetal Muscle Leg	muscle
14	chr13:63212400-63212600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr13:63212600-63213000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr13:63213000-63217000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr13:63217800-63219200	Enhancers	GM12878-XiMat	blood
18	chr13:63218000-63218400	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr13:63218000-63218600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr13:63218000-63218600	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr13:63218200-63218800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr13:63218400-63218600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr13:63231200-63231600	Active TSS	Spleen	Spleen
24	chr13:63235400-63235800	Enhancers	Fetal Heart	heart
25	chr13:63236000-63237400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr13:63236800-63238000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr13:63237200-63238000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr13:63237400-63237600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr13:63237600-63238600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr13:63239000-63239200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr13:63251800-63252600	Active TSS	A549	lung
32	chr13:63252200-63252600	Active TSS	Osteobl	bone
33	chr13:63252600-63252800	Flanking Active TSS	A549	lung
34	chr13:63263000-63265000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr13:63263200-63264400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr13:63263200-63266000	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr13:63263400-63264000	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr13:63263600-63264400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr13:63263600-63265200	Enhancers	iPS-18 Cell Line	embryonic stem cell
40	chr13:63264000-63264200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
41	chr13:63264000-63265800	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr13:63264200-63264600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr13:63264200-63264600	Enhancers	H9 Cell Line	embryonic stem cell
44	chr13:63264200-63264600	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr13:63264200-63265200	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr13:63264400-63264600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr13:63264600-63264800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr13:63264800-63265000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
49	chr13:63265000-63266000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr13:63266000-63266400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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