Variant report

Variant	nsv904420
Chromosome Location	chr15:78025267-78078903
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:682)
CpG islands
(count:306)
Chromatin interactive
region (count:47)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:682 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:78077195-78077543	K562	blood:	n/a	n/a
2	ARID3A	chr15:78029561-78030146	K562	blood:	n/a	n/a
3	ARID3A	chr15:78025169-78025381	K562	blood:	n/a	n/a
4	ARID3A	chr15:78026044-78026173	K562	blood:	n/a	n/a
5	ARID3A	chr15:78025705-78025756	K562	blood:	n/a	n/a
6	ATF3	chr15:78029970-78030172	K562	blood:	n/a	n/a
7	BACH1	chr15:78030635-78031074	K562	blood:	n/a	n/a
8	BCL11A	chr15:78031970-78032207	H1-hESC	embryonic stem cell:	n/a	n/a
9	BHLHE40	chr15:78045537-78045939	K562	blood:	n/a	n/a
10	BHLHE40	chr15:78025611-78025649	K562	blood:	n/a	n/a
11	BHLHE40	chr15:78077441-78077584	K562	blood:	n/a	n/a
12	BHLHE40	chr15:78026313-78026506	K562	blood:	n/a	n/a
13	BHLHE40	chr15:78040023-78040338	K562	blood:	n/a	n/a
14	BHLHE40	chr15:78029758-78030614	K562	blood:	n/a	n/a
15	BHLHE40	chr15:78027828-78027830	K562	blood:	n/a	n/a
16	BHLHE40	chr15:78024872-78025277	K562	blood:	n/a	n/a
17	CBX3	chr15:78077171-78077598	K562	blood:	n/a	n/a
18	CBX3	chr15:78029399-78030231	K562	blood:	n/a	n/a
19	CBX3	chr15:78052152-78052709	HCT-116	colon:	n/a	n/a
20	CCNT2	chr15:78025132-78025488	K562	blood:	n/a	n/a
21	CCNT2	chr15:78039480-78039819	K562	blood:	n/a	chr15:78039671-78039680
22	CCNT2	chr15:78031326-78031593	K562	blood:	n/a	chr15:78031399-78031408
23	CCNT2	chr15:78029729-78030559	K562	blood:	n/a	n/a
24	CEBPB	chr15:78039655-78039814	K562	blood:	n/a	n/a
25	CEBPB	chr15:78029819-78030279	K562	blood:	n/a	n/a
26	CEBPB	chr15:78044923-78044935	K562	blood:	n/a	n/a
27	CEBPB	chr15:78029777-78030350	K562	blood:	n/a	n/a
28	CEBPB	chr15:78048679-78048924	HepG2	liver:	n/a	chr15:78048788-78048799
29	CEBPB	chr15:78031992-78032232	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr15:78056910-78057263	K562	blood:	n/a	n/a
31	CEBPB	chr15:78044703-78044893	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr15:78048637-78048925	A549	lung:	n/a	chr15:78048788-78048799
33	CEBPB	chr15:78077418-78077509	K562	blood:	n/a	n/a
34	CEBPD	chr15:78029735-78030359	K562	blood:	n/a	n/a
35	CEBPD	chr15:78029730-78030349	K562	blood:	n/a	n/a
36	CHD1	chr15:78031753-78032303	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr15:78058928-78058962	K562	blood:	n/a	n/a
38	CREB1	chr15:78077295-78077568	A549	lung:	n/a	n/a
39	CTBP2	chr15:78031232-78032455	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr15:78077260-78077410	WI-38	lung:	n/a	n/a
41	CTCF	chr15:78077360-78077510	HPF	lung:	n/a	n/a
42	CTCF	chr15:78033236-78033296	MCF-7	breast:	n/a	n/a
43	CTCF	chr15:78077720-78077870	GM12866	blood:	n/a	n/a
44	CTCF	chr15:78077360-78077510	HL-60	blood:	n/a	n/a
45	CTCF	chr15:78077377-78077563	MCF-7	breast:	n/a	n/a
46	CTCF	chr15:78077400-78077550	HFF	foreskin:	n/a	n/a
47	CTCF	chr15:78077324-78077632	ECC-1	luminal epithelium:	n/a	n/a
48	CTCF	chr15:78077351-78077588	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr15:78031280-78031430	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr15:78077380-78077530	SAEC	small airway:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78077656-78077706	BJ	skin:	n/a
2	chr15:78077656-78077706	BJ	skin:	n/a
3	chr15:78077656-78077706	Caco-2	colon:	n/a
4	chr15:78025260-78025310	HIPEpiC	eye:	n/a
5	chr15:78031418-78031468	MCF10A-Er-Src	breast:	n/a
6	chr15:78060295-78060345	NHBE	bronchial:	n/a
7	chr15:78040120-78040170	LNCaP	prostate:	n/a
8	chr15:78025260-78025310	HCF	heart:	n/a
9	chr15:78060295-78060345	Jurkat	blood:	n/a
10	chr15:78077656-78077706	ECC-1	luminal epithelium:	n/a
11	chr15:78031418-78031468	ovcar-3	ovarian:	n/a
12	chr15:78077656-78077706	HCM	heart:	n/a
13	chr15:78077656-78077706	SK-N-SH_RA	brain:	n/a
14	chr15:78040120-78040170	AG04450	lung:	fetal
15	chr15:78077656-78077706	BE2_C	brain:	n/a
16	chr15:78060295-78060345	ECC-1	luminal epithelium:	n/a
17	chr15:78025260-78025310	HepG2	liver:	n/a
18	chr15:78040120-78040170	MCF10A-Er-Src	breast:	n/a
19	chr15:78025260-78025310	HNPCEpiC	eye:	n/a
20	chr15:78031418-78031468	HCPEpiC	choroid plexus:	n/a
21	chr15:78077656-78077706	ovcar-3	ovarian:	n/a
22	chr15:78025260-78025310	HCM	heart:	n/a
23	chr15:78040120-78040170	HPAEpiC	pulmonary alveolar:	n/a
24	chr15:78040120-78040170	GM12891	blood:	n/a
25	chr15:78040120-78040170	NB4	blood:	n/a
26	chr15:78040120-78040170	GM19239	blood:	n/a
27	chr15:78060295-78060345	H1-hESC	embryonic stem cell:	embryo
28	chr15:78060295-78060345	HRPEpiC	eye:	n/a
29	chr15:78031418-78031468	Hepatocyte	liver:	n/a
30	chr15:78031418-78031468	HMEC	breast:	n/a
31	chr15:78031418-78031468	AG09309	skin:	n/a
32	chr15:78025260-78025310	HEK293	kidney:	embryo
33	chr15:78025260-78025310	HRCEpiC	kidney:	n/a
34	chr15:78040120-78040170	MCF-7	breast:	n/a
35	chr15:78025260-78025310	AG04450	lung:	fetal
36	chr15:78040120-78040170	HRPEpiC	eye:	n/a
37	chr15:78025260-78025310	HCPEpiC	choroid plexus:	n/a
38	chr15:78060295-78060345	HAEpiC	amniotic membrane:	n/a
39	chr15:78025260-78025310	ovcar-3	ovarian:	n/a
40	chr15:78040120-78040170	Hepatocyte	liver:	n/a
41	chr15:78025260-78025310	GM06990	blood:	n/a
42	chr15:78077656-78077706	HUVEC	blood vessel:	n/a
43	chr15:78031418-78031468	HNPCEpiC	eye:	n/a
44	chr15:78031418-78031468	HCM	heart:	n/a
45	chr15:78040120-78040170	HIPEpiC	eye:	n/a
46	chr15:78077656-78077706	SAEC	small airway:	n/a
47	chr15:78040120-78040170	HCM	heart:	n/a
48	chr15:78060295-78060345	HEEpiC	esophagus:	n/a
49	chr15:78077656-78077706	AG04449	skin:	fetal
50	chr15:78031418-78031468	IMR90	lung:	fetal

(count:47 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:78022722..78024304-chr15:78040571..78043258,2	K562	blood:
2	chr15:77951815..77952789-chr15:78075941..78076556,2	K562	blood:
3	chr15:78049442..78052366-chr15:78052707..78054607,2	MCF-7	breast:
4	chr15:78044160..78046640-chr15:78075370..78077627,2	K562	blood:
5	chr15:78062199..78064857-chr15:78066773..78068430,2	K562	blood:
6	chr15:78029860..78033858-chr15:78038839..78041859,3	K562	blood:
7	chr15:78039556..78042296-chr15:78046861..78049587,2	K562	blood:
8	chr15:78022100..78024937-chr15:78029389..78030939,2	MCF-7	breast:
9	chr15:78025937..78028390-chr15:78028577..78030082,2	K562	blood:
10	chr15:78049309..78052245-chr15:78054880..78058301,3	K562	blood:
11	chr15:78037605..78040369-chr15:78045889..78047817,2	MCF-7	breast:
12	chr15:78028786..78030322-chr15:78031928..78034690,2	MCF-7	breast:
13	chr15:77925491..77927003-chr15:78065547..78066951,12	MCF-7	breast:
14	chr15:78062199..78064857-chr15:78066773..78068430,2	K562	blood:
15	chr15:78041656..78043427-chr15:78100097..78102130,2	MCF-7	breast:
16	chr15:78028786..78030322-chr15:78031928..78034690,2	MCF-7	breast:
17	chr15:78045800..78048382-chr15:78053626..78056901,3	K562	blood:
18	chr15:77925509..77926398-chr15:78076937..78077835,4	K562	blood:
19	chr15:77951783..77952314-chr15:78066187..78066759,2	MCF-7	breast:
20	chr15:78021356..78025369-chr15:78027266..78032240,6	K562	blood:
21	chr15:77951754..77952701-chr15:78076956..78077942,7	K562	blood:
22	chr15:78029999..78032267-chr15:78076792..78079270,2	MCF-7	breast:
23	chr15:78044160..78046640-chr15:78075370..78077627,2	K562	blood:
24	chr15:78029860..78033858-chr15:78038839..78041859,3	K562	blood:
25	chr15:78066595..78068537-chr15:78076215..78077798,2	K562	blood:
26	chr15:78034743..78037727-chr15:78038186..78041531,4	K562	blood:
27	chr15:78039556..78042296-chr15:78046861..78049587,2	K562	blood:
28	chr15:78059582..78063718-chr15:78064964..78067132,3	K562	blood:
29	chr15:78004582..78006437-chr15:78057929..78059969,2	MCF-7	breast:
30	chr15:78064180..78065710-chr15:78076746..78078989,2	K562	blood:
31	chr15:78021486..78023162-chr15:78023634..78026490,2	K562	blood:
32	chr15:78064180..78065710-chr15:78076746..78078989,2	K562	blood:
33	chr15:78037605..78040369-chr15:78045889..78047817,2	MCF-7	breast:
34	chr15:78025745..78027955-chr15:78030465..78032674,2	K562	blood:
35	chr15:78045800..78048382-chr15:78053626..78056901,3	K562	blood:
36	chr15:78049442..78052366-chr15:78052707..78054607,2	MCF-7	breast:
37	chr15:78059582..78063718-chr15:78064964..78067132,3	K562	blood:
38	chr15:77925532..77926425-chr15:78076783..78078398,4	MCF-7	breast:
39	chr15:78021356..78025369-chr15:78027266..78032240,6	K562	blood:
40	chr15:78033277..78034812-chr15:78040941..78043925,2	MCF-7	breast:
41	chr15:78049309..78052245-chr15:78054880..78058301,3	K562	blood:
42	chr15:78034743..78037727-chr15:78038186..78041531,4	K562	blood:
43	chr15:78066595..78068537-chr15:78076215..78077798,2	K562	blood:
44	chr15:78033277..78034812-chr15:78040941..78043925,2	MCF-7	breast:
45	chr15:78025937..78028390-chr15:78028577..78030082,2	K562	blood:
46	chr15:78025745..78027955-chr15:78030465..78032674,2	K562	blood:
47	chr15:78029999..78032267-chr15:78076792..78079270,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D2B-7	chr15:78027334-78027395	NONHSAT047458
2	lnc-TBC1D2B-7	chr15:78027334-78027395	NONHSAT047459
3	lnc-TBC1D2B-7	chr15:78027334-78027395	NONHSAT047460

No data

Variant related genes	Relation type
ENSG00000259213	TF binding region
ENSG00000259213	CpG island
ENSG00000259281	chromatin interactions
ENSG00000169783	chromatin interactions

Extended variants
information (count: 2081 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:2081 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4076999	chr15:78025267-78025268	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs532339342	chr15:78025290-78025291	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs547236002	chr15:78025334-78025335	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs4076998	chr15:78025420-78025421	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs62007780	chr15:78025464-78025465	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs4076997	chr15:78025468-78025469	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs556180150	chr15:78025477-78025478	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs79993924	chr15:78025508-78025509	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536613416	chr15:78025598-78025599	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs79022635	chr15:78025619-78025620	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564806021	chr15:78025627-78025628	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74868491	chr15:78025777-78025778	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs539229939	chr15:78025843-78025844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554109783	chr15:78025864-78025865	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs139424821	chr15:78025885-78025886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs56952924	chr15:78025893-78025894	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs149638395	chr15:78025921-78025922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs76879229	chr15:78025943-78025944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs543406971	chr15:78025944-78025945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs143907679	chr15:78026003-78026004	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78679308	chr15:78026099-78026100	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547867922	chr15:78026129-78026130	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148195511	chr15:78026192-78026193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370431655	chr15:78026193-78026194	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373675115	chr15:78026210-78026211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs529824450	chr15:78026243-78026244	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs148599673	chr15:78026247-78026248	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs10851896	chr15:78026325-78026326	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs536650196	chr15:78026333-78026334	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs143279072	chr15:78026353-78026354	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs141550025	chr15:78026367-78026368	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570415853	chr15:78026405-78026406	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs534464395	chr15:78026432-78026433	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs549079011	chr15:78026444-78026445	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs7174507	chr15:78026453-78026454	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs143151208	chr15:78026468-78026469	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs572696259	chr15:78026504-78026505	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs146686016	chr15:78026586-78026587	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs7174547	chr15:78026597-78026598	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs62007781	chr15:78026601-78026602	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs7179534	chr15:78026602-78026603	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs565180446	chr15:78026647-78026648	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs577148246	chr15:78026688-78026689	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs547593486	chr15:78026772-78026773	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs559386625	chr15:78026790-78026791	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs374970581	chr15:78026796-78026797	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs75008838	chr15:78026818-78026819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11301938	chr15:78026834-78026835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs576329309	chr15:78026914-78026915	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35722051	chr15:78026945-78026946	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78013000-78031200	Weak transcription	Fetal Brain Female	brain
2	chr15:78014000-78031000	Weak transcription	Spleen	Spleen
3	chr15:78020800-78030200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr15:78024800-78027000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:78025000-78025600	Weak transcription	Brain Angular Gyrus	brain
6	chr15:78025000-78025600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:78025000-78025800	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr15:78025200-78025400	Flanking Active TSS	K562	blood
9	chr15:78025400-78026400	Enhancers	K562	blood
10	chr15:78025400-78027600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr15:78025600-78025800	Enhancers	Brain Angular Gyrus	brain
12	chr15:78025600-78026400	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr15:78026200-78026400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr15:78026200-78026400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr15:78026200-78026400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr15:78026400-78026800	Flanking Active TSS	K562	blood
17	chr15:78026400-78029600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr15:78026800-78029400	Enhancers	K562	blood
19	chr15:78027000-78027600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr15:78027600-78028000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:78027600-78029800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr15:78028000-78029200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr15:78028200-78028400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
24	chr15:78028400-78028600	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr15:78028600-78029800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
26	chr15:78029200-78029400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr15:78029400-78029800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr15:78029400-78030600	Flanking Active TSS	K562	blood
29	chr15:78029600-78030400	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr15:78029800-78031000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr15:78029800-78031200	Enhancers	H9 Cell Line	embryonic stem cell
32	chr15:78029800-78031400	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr15:78029800-78031600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr15:78029800-78032800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr15:78030000-78030200	Enhancers	Colon Smooth Muscle	Colon
36	chr15:78030000-78030800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
37	chr15:78030000-78031200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr15:78030000-78031200	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
39	chr15:78030000-78031200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr15:78030000-78031600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
41	chr15:78030200-78033800	Enhancers	H1 Cell Line	embryonic stem cell
42	chr15:78030400-78031000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
43	chr15:78030400-78032000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr15:78030400-78032800	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chr15:78030600-78031200	Enhancers	Duodenum Mucosa	Duodenum
46	chr15:78030600-78033400	Enhancers	K562	blood
47	chr15:78030800-78031000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
48	chr15:78030800-78031400	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr15:78030800-78031400	Bivalent Enhancer	Fetal Brain Male	brain
50	chr15:78030800-78031400	Enhancers	Fetal Muscle Leg	muscle

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