Variant report

Variant	nsv900252
Chromosome Location	chr13:62502166-62687843
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	chr13:62612255-62612790	GM12878	blood:	n/a	n/a
2	ATF2	chr13:62612286-62612771	GM12878	blood:	n/a	n/a
3	BACH1	chr13:62684254-62684562	K562	blood:	n/a	n/a
4	BACH1	chr13:62684165-62684600	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr13:62612255-62612767	GM12878	blood:	n/a	chr13:62612558-62612567 chr13:62612580-62612590 chr13:62612469-62612480
6	BATF	chr13:62612376-62612741	GM12878	blood:	n/a	chr13:62612558-62612567 chr13:62612580-62612590 chr13:62612469-62612480
7	BCL11A	chr13:62612447-62612669	GM12878	blood:	n/a	chr13:62612582-62612591 chr13:62612583-62612592
8	BCL11A	chr13:62612280-62612716	GM12878	blood:	n/a	chr13:62612582-62612591 chr13:62612583-62612592
9	BRCA1	chr13:62528352-62528541	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr13:62564189-62564477	H1-hESC	embryonic stem cell:	n/a	chr13:62564307-62564318
11	CEBPB	chr13:62570699-62570994	HepG2	liver:	n/a	chr13:62570841-62570852
12	CEBPB	chr13:62610348-62610477	H1-hESC	embryonic stem cell:	n/a	chr13:62610382-62610393
13	CEBPB	chr13:62613007-62613244	HepG2	liver:	n/a	chr13:62613133-62613144 chr13:62613103-62613114
14	CEBPB	chr13:62618363-62618726	Hela-S3	cervix:	n/a	chr13:62618528-62618545 chr13:62618545-62618556 chr13:62618545-62618558 chr13:62618547-62618558
15	CEBPB	chr13:62667392-62667746	HepG2	liver:	n/a	chr13:62667563-62667576 chr13:62667564-62667575 chr13:62667563-62667574 chr13:62667563-62667576
16	CEBPB	chr13:62677940-62678189	HepG2	liver:	n/a	chr13:62678066-62678077
17	CEBPB	chr13:62667407-62667744	IMR90	lung:	n/a	chr13:62667563-62667576 chr13:62667564-62667575 chr13:62667563-62667574 chr13:62667563-62667576
18	CEBPB	chr13:62667407-62667625	K562	blood:	n/a	chr13:62667563-62667576 chr13:62667564-62667575 chr13:62667563-62667574 chr13:62667563-62667576
19	CEBPB	chr13:62610229-62610543	HepG2	liver:	n/a	chr13:62610382-62610393
20	CEBPB	chr13:62610264-62610555	IMR90	lung:	n/a	chr13:62610382-62610393
21	CEBPB	chr13:62576756-62577069	IMR90	lung:	n/a	chr13:62576888-62576899
22	CEBPB	chr13:62570732-62571005	A549	lung:	n/a	chr13:62570841-62570852
23	CEBPB	chr13:62667470-62667728	A549	lung:	n/a	chr13:62667563-62667576 chr13:62667564-62667575 chr13:62667563-62667574 chr13:62667563-62667576
24	CEBPB	chr13:62576732-62577043	HepG2	liver:	n/a	chr13:62576888-62576899
25	CEBPB	chr13:62612961-62613314	Hela-S3	cervix:	n/a	chr13:62613133-62613144 chr13:62613103-62613114
26	CEBPB	chr13:62564154-62564493	Hela-S3	cervix:	n/a	chr13:62564307-62564318
27	CEBPB	chr13:62617691-62618067	Hela-S3	cervix:	n/a	chr13:62617869-62617880
28	CEBPB	chr13:62564152-62564458	K562	blood:	n/a	chr13:62564307-62564318
29	CEBPB	chr13:62564130-62564492	HepG2	liver:	n/a	chr13:62564307-62564318
30	CEBPB	chr13:62564130-62564487	IMR90	lung:	n/a	chr13:62564307-62564318
31	CEBPB	chr13:62602465-62602672	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr13:62618394-62618675	HepG2	liver:	n/a	chr13:62618528-62618545 chr13:62618545-62618556 chr13:62618545-62618558 chr13:62618547-62618558
33	CEBPB	chr13:62617745-62617995	HepG2	liver:	n/a	chr13:62617869-62617880
34	CEBPB	chr13:62576755-62576995	A549	lung:	n/a	chr13:62576888-62576899
35	CHD2	chr13:62612415-62612482	GM12878	blood:	n/a	n/a
36	CTCF	chr13:62528340-62528490	GM06990	blood:	n/a	chr13:62528437-62528455 chr13:62528432-62528453 chr13:62528438-62528454
37	CTCF	chr13:62588480-62588630	HEEpiC	esophagus:	n/a	chr13:62588592-62588608 chr13:62588591-62588609 chr13:62588593-62588614
38	CTCF	chr13:62528242-62528708	MCF-7	breast:	n/a	chr13:62528437-62528455 chr13:62528432-62528453 chr13:62528438-62528454
39	CTCF	chr13:62528360-62528510	HepG2	liver:	n/a	chr13:62528437-62528455 chr13:62528432-62528453 chr13:62528438-62528454
40	CTCF	chr13:62528315-62528539	A549	lung:	n/a	chr13:62528437-62528455 chr13:62528432-62528453 chr13:62528438-62528454
41	CTCF	chr13:62528300-62528550	HCM	heart:	n/a	chr13:62528437-62528455 chr13:62528432-62528453 chr13:62528438-62528454
42	CTCF	chr13:62588538-62588680	HUVEC	blood vessel:	n/a	chr13:62588592-62588608 chr13:62588591-62588609 chr13:62588593-62588614
43	CTCF	chr13:62528380-62528530	RPTEC	kidney:	n/a	chr13:62528437-62528455 chr13:62528432-62528453 chr13:62528438-62528454
44	CTCF	chr13:62588480-62588630	HUVEC	blood vessel:	n/a	chr13:62588592-62588608 chr13:62588591-62588609 chr13:62588593-62588614
45	CTCF	chr13:62588620-62588770	RPTEC	kidney:	n/a	n/a
46	CTCF	chr13:62528300-62528450	NHEK	skin:	n/a	n/a
47	CTCF	chr13:62528294-62528603	IMR90	lung:	n/a	chr13:62528437-62528455 chr13:62528432-62528453 chr13:62528438-62528454
48	CTCF	chr13:62588435-62588693	HepG2	liver:	n/a	chr13:62588592-62588608 chr13:62588591-62588609 chr13:62588593-62588614
49	CTCF	chr13:62623831-62623899	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr13:62588540-62588690	HRPEpiC	eye:	n/a	chr13:62588592-62588608 chr13:62588591-62588609 chr13:62588593-62588614

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:62516636-62516686	IMR90	lung:	fetal
2	chr13:62516636-62516686	IMR90	lung:	fetal
3	chr13:62516636-62516686	NT2-D1	testis:	n/a
4	chr13:62515965-62516015	SKMC	muscle:	n/a
5	chr13:62516040-62516090	HCPEpiC	choroid plexus:	n/a
6	chr13:62516040-62516090	PrEC	prostate:	n/a
7	chr13:62515965-62516015	MCF10A-Er-Src	breast:	n/a
8	chr13:62516163-62516213	NH-A	brain:	n/a
9	chr13:62515965-62516015	A549	lung:	n/a
10	chr13:62515965-62516015	NHBE	bronchial:	n/a
11	chr13:62516636-62516686	GM12891	blood:	n/a
12	chr13:62515876-62515926	MCF-7	breast:	n/a
13	chr13:62516163-62516213	SK-N-MC	brain:	n/a
14	chr13:62516113-62516163	NHBE	bronchial:	n/a
15	chr13:62515876-62515926	HCM	heart:	n/a
16	chr13:62515965-62516015	GM12891	blood:	n/a
17	chr13:62516113-62516163	ProgFib	skin:	n/a
18	chr13:62515965-62516015	MCF-7	breast:	n/a
19	chr13:62515876-62515926	AG10803	skin:	n/a
20	chr13:62516636-62516686	Hepatocyte	liver:	n/a
21	chr13:62516580-62516630	HCM	heart:	n/a
22	chr13:62516113-62516163	RPTEC	kidney:	n/a
23	chr13:62516113-62516163	GM12892	blood:	n/a
24	chr13:62515965-62516015	HEEpiC	esophagus:	n/a
25	chr13:62516040-62516090	ProgFib	skin:	n/a
26	chr13:62516113-62516163	ovcar-3	ovarian:	n/a
27	chr13:62516163-62516213	SAEC	small airway:	n/a
28	chr13:62516636-62516686	LNCaP	prostate:	n/a
29	chr13:62516113-62516163	NH-A	brain:	n/a
30	chr13:62515876-62515926	AG04449	skin:	fetal
31	chr13:62516163-62516213	U87	brain:	n/a
32	chr13:62516580-62516630	Hepatocyte	liver:	n/a
33	chr13:62516636-62516686	HAEpiC	amniotic membrane:	n/a
34	chr13:62515965-62516015	AoSMC	blood vessel:	n/a
35	chr13:62516580-62516630	HNPCEpiC	eye:	n/a
36	chr13:62516163-62516213	ECC-1	luminal epithelium:	n/a
37	chr13:62516580-62516630	Caco-2	colon:	n/a
38	chr13:62516636-62516686	GM19239	blood:	n/a
39	chr13:62516636-62516686	NHDF-neo	bronchial:	n/a
40	chr13:62516040-62516090	AG10803	skin:	n/a
41	chr13:62515876-62515926	GM19239	blood:	n/a
42	chr13:62516040-62516090	GM19239	blood:	n/a
43	chr13:62516040-62516090	Jurkat	blood:	n/a
44	chr13:62516163-62516213	MCF10A-Er-Src	breast:	n/a
45	chr13:62516040-62516090	NHBE	bronchial:	n/a
46	chr13:62516580-62516630	HepG2	liver:	n/a
47	chr13:62516163-62516213	HCM	heart:	n/a
48	chr13:62515965-62516015	HCT-116	colon:	n/a
49	chr13:62516636-62516686	GM12892	blood:	n/a
50	chr13:62516040-62516090	AG04450	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr13:62454695..62455293-chr13:62527943..62528961,3	MCF-7	breast:
2	chr13:62660162..62662545-chr13:62664101..62665603,2	K562	blood:
3	chr13:62629003..62630870-chr13:62631418..62633606,2	MCF-7	breast:
4	chr13:62595210..62597169-chr17:57923317..57925100,2	MCF-7	breast:
5	chr13:62549291..62551887-chr13:62564768..62566539,2	K562	blood:
6	chr13:62660162..62662545-chr13:62664101..62665603,2	K562	blood:
7	chr13:62454539..62455596-chr13:62527363..62528851,4	MCF-7	breast:
8	chr13:62629003..62630870-chr13:62631418..62633606,2	MCF-7	breast:
9	chr13:62588294..62590815-chr13:62591297..62594105,2	K562	blood:
10	chr13:62549291..62551887-chr13:62564768..62566539,2	K562	blood:
11	chr13:62588294..62590815-chr13:62591297..62594105,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH20-1	chr13:62577291-62577307	NONHSAT034137
2	lnc-PCDH20-1	chr13:62599517-62599614	XLOC_010635
3	lnc-PCDH20-1	chr13:62603392-62603681	NONHSAT034137
4	lnc-PCDH20-1	chr13:62577658-62578643	NR_046995
5	lnc-PCDH20-1	chr13:62578267-62578643	XLOC_010635
6	lnc-PCDH20-14	chr13:62666624-62666665	NONHSAT034139
7	lnc-PCDH20-1	chr13:62578226-62578643	XLOC_010635
8	lnc-PCDH20-1	chr13:62603392-62603681	XLOC_010635
9	lnc-PCDH20-1	chr13:62577659-62578643	NONHSAT034137
10	lnc-PCDH20-14	chr13:62655235-62655462	NONHSAT034139
11	lnc-PCDH20-1	chr13:62603392-62603681	NR_046995

Variant related genes	Relation type
ENSG00000270856	TF binding region
LINC00358	TF binding region
ENSG00000270856	CpG island
LINC00358	CpG island
ENSG00000201524	chromatin interactions

Extended variants
information (count: 1640 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1640 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1332388	chr13:62502166-62502167	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140754353	chr13:62502207-62502208	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs183644871	chr13:62502259-62502260	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs1332389	chr13:62502311-62502312	Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs564442422	chr13:62502342-62502343	Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs10708167	chr13:62504031-62504032	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs398023057	chr13:62504034-62504035	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs139180461	chr13:62504045-62504046	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs539411930	chr13:62504068-62504069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs532694188	chr13:62504119-62504120	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs77141549	chr13:62504152-62504153	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs146420967	chr13:62504175-62504176	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs181897476	chr13:62504200-62504201	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs140748883	chr13:62504221-62504222	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs371961044	chr13:62504263-62504264	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs560545734	chr13:62504286-62504287	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs528642190	chr13:62504337-62504338	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs552472781	chr13:62504339-62504340	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs184880483	chr13:62504357-62504358	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs546173755	chr13:62504409-62504410	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs4884404	chr13:62504410-62504411	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs189785951	chr13:62504505-62504506	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs534912709	chr13:62504506-62504507	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs549974621	chr13:62504518-62504519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs182934826	chr13:62504529-62504530	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs548615030	chr13:62504536-62504537	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs568503811	chr13:62504549-62504550	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs537429308	chr13:62504567-62504568	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs529554901	chr13:62504643-62504644	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs546649283	chr13:62504701-62504702	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs60227683	chr13:62504702-62504703	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs397815230	chr13:62504711-62504712	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs547726262	chr13:62504712-62504713	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs557275349	chr13:62504723-62504724	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs566361343	chr13:62504753-62504754	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs7999333	chr13:62504780-62504781	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs201937913	chr13:62504819-62504820	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs111918744	chr13:62504853-62504854	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs569667456	chr13:62504861-62504862	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs147983242	chr13:62504903-62504904	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs375044844	chr13:62504904-62504905	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs186694429	chr13:62504914-62504915	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs376665805	chr13:62504922-62504923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs150259308	chr13:62504971-62504972	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs191574318	chr13:62504981-62504982	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs183825650	chr13:62504990-62504991	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs116485794	chr13:62504992-62504993	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs77414217	chr13:62505009-62505010	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs145870858	chr13:62505010-62505011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs187545508	chr13:62505032-62505033	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
small cell lung cancer	20016488	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:74 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:62502000-62502400	Flanking Active TSS	HUVEC	blood vessel
2	chr13:62510000-62510400	Enhancers	GM12878-XiMat	blood
3	chr13:62524200-62524600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
4	chr13:62547200-62548400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr13:62547400-62548200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr13:62547800-62548200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr13:62549200-62550000	Enhancers	Fetal Lung	lung
8	chr13:62562800-62563200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr13:62578400-62578600	Enhancers	Pancreas	Pancrea
10	chr13:62585400-62585800	Enhancers	Fetal Heart	heart
11	chr13:62588400-62588600	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr13:62588600-62588800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
13	chr13:62588600-62589000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr13:62588600-62589000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr13:62588600-62589000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr13:62588600-62589000	Active TSS	Adipose Nuclei	Adipose
17	chr13:62588600-62589000	Active TSS	Brain Angular Gyrus	brain
18	chr13:62588600-62589000	Active TSS	Brain Anterior Caudate	brain
19	chr13:62588600-62589000	Active TSS	Brain Cingulate Gyrus	brain
20	chr13:62588600-62589000	Active TSS	Brain Hippocampus Middle	brain
21	chr13:62588600-62589000	Active TSS	Brain Inferior Temporal Lobe	brain
22	chr13:62588600-62589000	Active TSS	Brain Substantia Nigra	brain
23	chr13:62588600-62589000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
24	chr13:62588600-62589000	Active TSS	Fetal Lung	lung
25	chr13:62588600-62589000	Active TSS	Fetal Muscle Leg	muscle
26	chr13:62588600-62589000	Active TSS	Fetal Stomach	stomach
27	chr13:62588600-62589000	Active TSS	Psoas Muscle	Psoas
28	chr13:62588600-62589000	Active TSS	A549	lung
29	chr13:62588600-62589000	Active TSS	Hela-S3	cervix
30	chr13:62594600-62595400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:62603400-62603800	Enhancers	Brain Anterior Caudate	brain
32	chr13:62603600-62604000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr13:62604000-62606400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr13:62605200-62605800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr13:62605200-62605800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr13:62605600-62606000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr13:62605600-62606000	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr13:62605800-62607800	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr13:62606000-62607400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr13:62607400-62607800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr13:62607800-62608200	Enhancers	Brain Hippocampus Middle	brain
42	chr13:62607800-62608400	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr13:62608200-62608600	Active TSS	Brain Hippocampus Middle	brain
44	chr13:62612200-62612800	Enhancers	GM12878-XiMat	blood
45	chr13:62620400-62621200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr13:62620600-62621200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr13:62621200-62626600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr13:62625600-62626200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr13:62639000-62639800	Enhancers	Fetal Lung	lung
50	chr13:62642400-62643000	Active TSS	Fetal Kidney	kidney

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