Variant report

Variant	nsv471162
Chromosome Location	chr13:85994700-86296819
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	ATF3	chr13:86160565-86161037	A549	lung:	n/a	n/a
2	BACH1	chr13:86239351-86239684	K562	blood:	n/a	chr13:86239558-86239572
3	BACH1	chr13:86009114-86009355	H1-hESC	embryonic stem cell:	n/a	chr13:86009260-86009274
4	BACH1	chr13:86249505-86249834	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr13:86239351-86239763	H1-hESC	embryonic stem cell:	n/a	chr13:86239558-86239572
6	BACH1	chr13:86129617-86129727	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL11A	chr13:86142106-86142365	H1-hESC	embryonic stem cell:	n/a	n/a
8	BCL3	chr13:86102638-86103148	A549	lung:	n/a	n/a
9	BCL3	chr13:86086502-86086960	A549	lung:	n/a	n/a
10	BHLHE40	chr13:86191746-86192046	GM12878	blood:	n/a	n/a
11	BHLHE40	chr13:86239577-86239690	GM12878	blood:	n/a	n/a
12	BRCA1	chr13:86071289-86072157	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr13:86006029-86006048	HepG2	liver:	n/a	n/a
14	BRCA1	chr13:86102651-86103573	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr13:86181314-86181618	HepG2	liver:	n/a	chr13:86181454-86181465
16	CEBPB	chr13:86102695-86103049	A549	lung:	n/a	chr13:86102839-86102850 chr13:86102886-86102903 chr13:86102839-86102850
17	CEBPB	chr13:86016784-86017068	Hela-S3	cervix:	n/a	chr13:86016932-86016943
18	CEBPB	chr13:86083228-86083529	MCF-7	breast:	n/a	n/a
19	CEBPB	chr13:86104242-86104613	IMR90	lung:	n/a	chr13:86104432-86104445 chr13:86104418-86104429
20	CEBPB	chr13:86293299-86293606	MCF-7	breast:	n/a	chr13:86293460-86293471 chr13:86293461-86293472 chr13:86293460-86293473 chr13:86293462-86293471 chr13:86293460-86293473
21	CEBPB	chr13:86068032-86068227	A549	lung:	n/a	chr13:86068112-86068123
22	CEBPB	chr13:86283208-86283506	MCF-7	breast:	n/a	n/a
23	CEBPB	chr13:86104252-86104599	HepG2	liver:	n/a	chr13:86104432-86104445 chr13:86104418-86104429
24	CEBPB	chr13:86181411-86181492	H1-hESC	embryonic stem cell:	n/a	chr13:86181454-86181465
25	CEBPB	chr13:86160593-86160895	MCF-7	breast:	n/a	n/a
26	CEBPB	chr13:86172257-86172602	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr13:86181383-86181620	A549	lung:	n/a	chr13:86181454-86181465
28	CEBPB	chr13:86238060-86238356	A549	lung:	n/a	chr13:86238215-86238224 chr13:86238215-86238226 chr13:86238213-86238226 chr13:86238213-86238224
29	CEBPB	chr13:86071389-86072263	Hela-S3	cervix:	n/a	chr13:86071803-86071820
30	CEBPB	chr13:86290318-86290618	IMR90	lung:	n/a	chr13:86290443-86290454
31	CEBPB	chr13:86283179-86283525	A549	lung:	n/a	n/a
32	CEBPB	chr13:86283143-86283584	A549	lung:	n/a	n/a
33	CEBPB	chr13:86162587-86162846	A549	lung:	n/a	chr13:86162681-86162692 chr13:86162681-86162694
34	CEBPB	chr13:86110856-86111237	IMR90	lung:	n/a	n/a
35	CEBPB	chr13:86293378-86293532	K562	blood:	n/a	chr13:86293460-86293471 chr13:86293461-86293472 chr13:86293460-86293473 chr13:86293462-86293471 chr13:86293460-86293473
36	CEBPB	chr13:86293332-86293643	IMR90	lung:	n/a	chr13:86293460-86293471 chr13:86293461-86293472 chr13:86293460-86293473 chr13:86293462-86293471 chr13:86293460-86293473
37	CEBPB	chr13:86293320-86293622	A549	lung:	n/a	chr13:86293460-86293471 chr13:86293461-86293472 chr13:86293460-86293473 chr13:86293462-86293471 chr13:86293460-86293473
38	CEBPB	chr13:86283931-86284111	MCF-7	breast:	n/a	chr13:86283993-86284005
39	CEBPB	chr13:86068041-86068241	HepG2	liver:	n/a	chr13:86068112-86068123
40	CEBPB	chr13:86192278-86192537	HepG2	liver:	n/a	chr13:86192375-86192388 chr13:86192376-86192387
41	CEBPB	chr13:86162521-86162852	IMR90	lung:	n/a	chr13:86162681-86162692 chr13:86162681-86162694
42	CEBPB	chr13:86238068-86238374	IMR90	lung:	n/a	chr13:86238215-86238224 chr13:86238215-86238226 chr13:86238213-86238226 chr13:86238213-86238224
43	CEBPB	chr13:86102562-86103728	Hela-S3	cervix:	n/a	chr13:86102839-86102850 chr13:86102886-86102903 chr13:86102839-86102850
44	CEBPB	chr13:86071555-86072281	IMR90	lung:	n/a	chr13:86071803-86071820
45	CEBPB	chr13:86102639-86103686	IMR90	lung:	n/a	chr13:86102839-86102850 chr13:86102886-86102903 chr13:86102839-86102850
46	CEBPB	chr13:86083260-86083477	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr13:86275089-86275377	HepG2	liver:	n/a	chr13:86275273-86275284 chr13:86275271-86275282
48	CEBPB	chr13:86001587-86001888	Hela-S3	cervix:	n/a	chr13:86001689-86001700
49	CEBPB	chr13:86071751-86072088	A549	lung:	n/a	chr13:86071803-86071820
50	CEBPB	chr13:86102631-86103205	A549	lung:	n/a	chr13:86102839-86102850 chr13:86102886-86102903 chr13:86102839-86102850

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:86268291-86268341	SK-N-SH	brain:	n/a
2	chr13:86268291-86268341	AoSMC	blood vessel:	n/a
3	chr13:86238596-86238646	NT2-D1	testis:	n/a
4	chr13:86268291-86268341	NH-A	brain:	n/a
5	chr13:86140055-86140105	HNPCEpiC	eye:	n/a
6	chr13:86268291-86268341	GM06990	blood:	n/a
7	chr13:86268291-86268341	NB4	blood:	n/a
8	chr13:86140055-86140105	HMEC	breast:	n/a
9	chr13:86268291-86268341	HEK293	kidney:	embryo
10	chr13:86238596-86238646	HEK293	kidney:	embryo
11	chr13:86140055-86140105	HEEpiC	esophagus:	n/a
12	chr13:86268291-86268341	NHBE	bronchial:	n/a
13	chr13:86140055-86140105	Hepatocyte	liver:	n/a
14	chr13:86268291-86268341	AG10803	skin:	n/a
15	chr13:86140055-86140105	HRCEpiC	kidney:	n/a
16	chr13:86268291-86268341	LNCaP	prostate:	n/a
17	chr13:86238596-86238646	ProgFib	skin:	n/a
18	chr13:86238596-86238646	NHBE	bronchial:	n/a
19	chr13:86140055-86140105	ECC-1	luminal epithelium:	n/a
20	chr13:86268291-86268341	HCM	heart:	n/a
21	chr13:86238596-86238646	HAEpiC	amniotic membrane:	n/a
22	chr13:86268291-86268341	HL-60	blood:	n/a
23	chr13:86268291-86268341	Caco-2	colon:	n/a
24	chr13:86238596-86238646	NH-A	brain:	n/a
25	chr13:86238596-86238646	HMEC	breast:	n/a
26	chr13:86238596-86238646	HPAEpiC	pulmonary alveolar:	n/a
27	chr13:86238596-86238646	MCF-7	breast:	n/a
28	chr13:86268291-86268341	MCF-7	breast:	n/a
29	chr13:86268291-86268341	NT2-D1	testis:	n/a
30	chr13:86238596-86238646	K562	blood:	n/a
31	chr13:86140055-86140105	K562	blood:	n/a
32	chr13:86268291-86268341	MCF10A-Er-Src	breast:	n/a
33	chr13:86238596-86238646	Caco-2	colon:	n/a
34	chr13:86238596-86238646	HRE	kidney:	n/a
35	chr13:86268291-86268341	U87	brain:	n/a
36	chr13:86238596-86238646	NHDF-neo	bronchial:	n/a
37	chr13:86140055-86140105	NHBE	bronchial:	n/a
38	chr13:86140055-86140105	Hela-S3	cervix:	n/a
39	chr13:86268291-86268341	ProgFib	skin:	n/a
40	chr13:86140055-86140105	U87	brain:	n/a
41	chr13:86238596-86238646	Hela-S3	cervix:	n/a
42	chr13:86140055-86140105	SKMC	muscle:	n/a
43	chr13:86268291-86268341	IMR90	lung:	fetal
44	chr13:86140055-86140105	BJ	skin:	n/a
45	chr13:86268291-86268341	AG04450	lung:	fetal
46	chr13:86238596-86238646	CMK	blood:	n/a
47	chr13:86140055-86140105	NH-A	brain:	n/a
48	chr13:86140055-86140105	SK-N-SH_RA	brain:	n/a
49	chr13:86238596-86238646	ovcar-3	ovarian:	n/a
50	chr13:86238596-86238646	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:86099181..86102107-chr13:86106453..86108708,2	MCF-7	breast:
2	chr13:86279490..86281664-chr13:86283799..86286531,3	MCF-7	breast:
3	chr13:86281640..86283292-chr13:86288920..86291298,2	MCF-7	breast:
4	chr13:86096125..86097964-chr13:86110495..86113341,2	MCF-7	breast:
5	chr13:86081905..86084326-chr13:86372446..86374070,2	MCF-7	breast:
6	chr13:86078290..86080136-chr13:86083159..86084884,2	MCF-7	breast:
7	chr13:86099181..86102107-chr13:86106453..86108708,2	MCF-7	breast:
8	chr13:86281640..86283292-chr13:86288920..86291298,2	MCF-7	breast:
9	chr13:86033358..86036212-chr13:86039864..86042849,2	MCF-7	breast:
10	chr13:86012041..86014222-chr13:86015485..86017247,2	K562	blood:
11	chr13:86279490..86281664-chr13:86283799..86286531,3	MCF-7	breast:
12	chr13:86155275..86157872-chr13:86359223..86361897,2	MCF-7	breast:
13	chr13:86160634..86163569-chr13:86372135..86374824,2	MCF-7	breast:
14	chr13:86033358..86036212-chr13:86039864..86042849,2	MCF-7	breast:
15	chr13:86096125..86097964-chr13:86110495..86113341,2	MCF-7	breast:
16	chr13:86078290..86080136-chr13:86083159..86084884,2	MCF-7	breast:
17	chr13:86164717..86166503-chr13:86370230..86372028,2	MCF-7	breast:
18	chr13:86226206..86227148-chr9:80190237..80190893,2	MCF-7	breast:
19	chr13:86012041..86014222-chr13:86015485..86017247,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-1	chr13:86205771-86205977	XLOC_010681
2	lnc-SLITRK5-11	chr13:86107209-86107338	XLOC_010460
3	lnc-SLITRK5-11	chr13:86107211-86107338	NONHSAT034564
4	lnc-SLITRK5-11	chr13:86116373-86116465	XLOC_010460
5	lnc-SLITRK5-30	chr13:86240824-86240895	NONHSAT034569
6	lnc-SLITRK5-30	chr13:86270269-86270344	NONHSAT034569
7	lnc-SLITRK5-11	chr13:86118511-86118797	NONHSAT034564
8	lnc-SLITRK5-11	chr13:86107211-86107338	ENSG00000226317.2
9	lnc-SLITRK5-11	chr13:86116373-86116465	ENSG00000226317.2
10	lnc-SLITRK5-11	chr13:86116373-86116465	NONHSAT034564
11	lnc-SLITRK6-1	chr13:86215835-86216180	XLOC_010681
12	lnc-SLITRK5-30	chr13:86250665-86250748	NONHSAT034569
13	lnc-SLITRK6-1	chr13:86215835-86215991	XLOC_010681
14	lnc-SLITRK6-1	chr13:86205874-86205977	XLOC_010681
15	lnc-SLITRK6-1	chr13:86203729-86203774	XLOC_010681
16	lnc-SLITRK5-11	chr13:86118511-86118705	XLOC_010460
17	lnc-SLITRK5-11	chr13:86118511-86118705	ENSG00000226317.2

Variant related genes	Relation type
RNU6-72P	TF binding region
RNU6-72P	CpG island
ENSG00000184564	chromatin interactions
CELSR3	miRNA target sites

Extended variants
information (count: 7757 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:7757 , 50 per page) page: 1 2 3 4 5 6 7 ... 156

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9547210	chr13:85994700-85994701	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564467901	chr13:85994708-85994709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531833427	chr13:85994757-85994758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549819242	chr13:85994775-85994776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs539382175	chr13:85994782-85994783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77823055	chr13:85994810-85994811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs548868932	chr13:85994858-85994859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs17079795	chr13:85994876-85994877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs61971216	chr13:85994943-85994944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146169963	chr13:85995078-85995079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs183209088	chr13:85995088-85995089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs140206748	chr13:85995120-85995121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369278598	chr13:85995201-85995202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs576716846	chr13:85995217-85995218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs537956065	chr13:85995277-85995278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs556263213	chr13:85995329-85995330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs11618050	chr13:85995354-85995355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs527903724	chr13:85995363-85995364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs552531505	chr13:85995366-85995367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542025837	chr13:85995374-85995375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs372970048	chr13:85995389-85995390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560474568	chr13:85995396-85995397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs572299910	chr13:85995423-85995424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs545730861	chr13:85995441-85995442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564512348	chr13:85995442-85995443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs570590734	chr13:85995444-85995445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs375169788	chr13:85995451-85995452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555504674	chr13:85995567-85995568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143894167	chr13:85995578-85995579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs146375369	chr13:85995608-85995609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs17462219	chr13:85995671-85995672	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs532518299	chr13:85995672-85995673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549755293	chr13:85995690-85995691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187896750	chr13:85995705-85995706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568122590	chr13:85995708-85995709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs551746734	chr13:85995718-85995719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs570446129	chr13:85995754-85995755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs192011430	chr13:85995773-85995774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs139368851	chr13:85995787-85995788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs568147767	chr13:85995789-85995790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs150026081	chr13:85995790-85995791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs78605164	chr13:85995796-85995797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs71440180	chr13:85995800-85995801	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs572103091	chr13:85995868-85995869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs1854888	chr13:85995893-85995894	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs145251831	chr13:85995933-85995934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576411820	chr13:85996011-85996012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543395353	chr13:85996017-85996018	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs149151851	chr13:85996023-85996024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529345354	chr13:85996024-85996025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
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
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	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	19490664	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-small cell lung cancer	16651412	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:85986200-86001400	Weak transcription	Fetal Lung	lung
2	chr13:86001200-86001600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:86001400-86001800	Enhancers	Fetal Lung	lung
4	chr13:86002200-86004600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr13:86004800-86005000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
6	chr13:86005000-86005200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:86005200-86005400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr13:86005200-86005600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr13:86005400-86006200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr13:86006000-86006200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr13:86014000-86014200	Enhancers	A549	lung
12	chr13:86014200-86015000	Weak transcription	A549	lung
13	chr13:86015000-86015200	Enhancers	A549	lung
14	chr13:86015200-86016200	Active TSS	A549	lung
15	chr13:86022800-86024400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
16	chr13:86023000-86024600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr13:86023200-86023800	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr13:86023200-86024200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr13:86023400-86023600	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr13:86023400-86024200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr13:86023600-86023800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
22	chr13:86023600-86024400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr13:86023800-86024000	Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr13:86024000-86024200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr13:86024400-86028000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr13:86031800-86032200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr13:86032200-86033800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr13:86032800-86033200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr13:86033800-86034600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr13:86034600-86035200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr13:86036000-86037000	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr13:86054000-86054400	Enhancers	Fetal Heart	heart
33	chr13:86060800-86061200	Enhancers	Duodenum Smooth Muscle	Duodenum
34	chr13:86065800-86066600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr13:86066200-86066800	Enhancers	Fetal Heart	heart
36	chr13:86069200-86077200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr13:86070600-86071400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr13:86070600-86071600	Enhancers	NHLF	lung
39	chr13:86070600-86071800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr13:86070600-86072800	Enhancers	Hela-S3	cervix
41	chr13:86070800-86071800	Enhancers	NH-A	brain
42	chr13:86071200-86071400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr13:86071200-86071600	Enhancers	NHEK	skin
44	chr13:86071200-86073000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr13:86071400-86071800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr13:86071400-86073400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr13:86071600-86072000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr13:86071600-86072000	Flanking Active TSS	NHEK	skin
49	chr13:86071600-86072400	Weak transcription	NHLF	lung
50	chr13:86071800-86072600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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