Variant report

Variant	nsv904422
Chromosome Location	chr15:78055479-78106177
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:493)
CpG islands
(count:183)
Chromatin interactive
region (count:39)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:493 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	BCL3	chr15:78088304-78088829	GM12878	blood:	n/a	n/a
3	BCL3	chr15:78088327-78088760	GM12878	blood:	n/a	n/a
4	BHLHE40	chr15:78102084-78102117	K562	blood:	n/a	n/a
5	BHLHE40	chr15:78104173-78104542	K562	blood:	n/a	chr15:78104303-78104324 chr15:78104308-78104317 chr15:78104309-78104318 chr15:78104310-78104319 chr15:78104309-78104318 chr15:78104307-78104320
6	BHLHE40	chr15:78096532-78096945	K562	blood:	n/a	n/a
7	BHLHE40	chr15:78101148-78101512	HepG2	liver:	n/a	chr15:78101316-78101325 chr15:78101317-78101326 chr15:78101317-78101326
8	BHLHE40	chr15:78101143-78101495	K562	blood:	n/a	chr15:78101316-78101325 chr15:78101317-78101326 chr15:78101317-78101326
9	BHLHE40	chr15:78077441-78077584	K562	blood:	n/a	n/a
10	BHLHE40	chr15:78089629-78089938	GM12878	blood:	n/a	n/a
11	BHLHE40	chr15:78095857-78096131	K562	blood:	n/a	n/a
12	CBX3	chr15:78077171-78077598	K562	blood:	n/a	n/a
13	CEBPB	chr15:78097972-78098198	Hela-S3	cervix:	n/a	chr15:78098032-78098043
14	CEBPB	chr15:78097885-78098211	K562	blood:	n/a	chr15:78098032-78098043
15	CEBPB	chr15:78097916-78098237	MCF-7	breast:	n/a	chr15:78098032-78098043
16	CEBPB	chr15:78097908-78098155	H1-hESC	embryonic stem cell:	n/a	chr15:78098032-78098043
17	CEBPB	chr15:78097862-78098204	HepG2	liver:	n/a	chr15:78098032-78098043
18	CEBPB	chr15:78077418-78077509	K562	blood:	n/a	n/a
19	CEBPB	chr15:78056910-78057263	K562	blood:	n/a	n/a
20	CEBPB	chr15:78097866-78098207	IMR90	lung:	n/a	chr15:78098032-78098043
21	CEBPB	chr15:78097872-78098202	A549	lung:	n/a	chr15:78098032-78098043
22	CHD2	chr15:78095843-78096168	K562	blood:	n/a	n/a
23	CHD2	chr15:78058928-78058962	K562	blood:	n/a	n/a
24	CHD2	chr15:78093119-78093139	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr15:78089582-78089843	GM12878	blood:	n/a	n/a
26	CREB1	chr15:78077295-78077568	A549	lung:	n/a	n/a
27	CTCF	chr15:78077360-78077510	HCM	heart:	n/a	n/a
28	CTCF	chr15:78077380-78077530	AG09309	skin:	n/a	n/a
29	CTCF	chr15:78078280-78078430	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr15:78077353-78077586	A549	lung:	n/a	n/a
31	CTCF	chr15:78060300-78060450	K562	blood:	n/a	n/a
32	CTCF	chr15:78066159-78066739	MCF-7	breast:	n/a	chr15:78066293-78066302 chr15:78066246-78066259
33	CTCF	chr15:78102200-78102350	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr15:78060500-78060896	K562	blood:	n/a	n/a
35	CTCF	chr15:78091920-78092070	GM12873	blood:	n/a	n/a
36	CTCF	chr15:78077324-78077632	ECC-1	luminal epithelium:	n/a	n/a
37	CTCF	chr15:78066344-78066553	MCF-7	breast:	n/a	n/a
38	CTCF	chr15:78077394-78077590	SK-N-SH_RA	brain:	n/a	n/a
39	CTCF	chr15:78066156-78066728	HCT-116	colon:	n/a	chr15:78066293-78066302 chr15:78066246-78066259
40	CTCF	chr15:78077376-78077589	GM19239	blood:	n/a	n/a
41	CTCF	chr15:78077760-78077910	GM12867	blood:	n/a	n/a
42	CTCF	chr15:78086344-78086366	Kidney_OC	kidney:	n/a	n/a
43	CTCF	chr15:78077420-78077570	HCT-116	colon:	n/a	n/a
44	CTCF	chr15:78077380-78077530	GM12867	blood:	n/a	n/a
45	CTCF	chr15:78077153-78077163	GM12892	blood:	n/a	n/a
46	CTCF	chr15:78104520-78104670	HepG2	liver:	n/a	n/a
47	CTCF	chr15:78077340-78077490	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr15:78077380-78077530	AG10803	skin:	n/a	n/a
49	CTCF	chr15:78077380-78077530	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr15:78077440-78077590	HRE	kidney:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78077656-78077706	SK-N-MC	brain:	n/a
2	chr15:78103228-78103278	AG04450	lung:	fetal
3	chr15:78060295-78060345	GM12878	blood:	n/a
4	chr15:78060295-78060345	IMR90	lung:	fetal
5	chr15:78060295-78060345	NH-A	brain:	n/a
6	chr15:78103228-78103278	ECC-1	luminal epithelium:	n/a
7	chr15:78077656-78077706	HCPEpiC	choroid plexus:	n/a
8	chr15:78060295-78060345	SK-N-MC	brain:	n/a
9	chr15:78077656-78077706	HEK293	kidney:	embryo
10	chr15:78103228-78103278	HPAEpiC	pulmonary alveolar:	n/a
11	chr15:78077656-78077706	HMEC	breast:	n/a
12	chr15:78077656-78077706	LNCaP	prostate:	n/a
13	chr15:78060295-78060345	LNCaP	prostate:	n/a
14	chr15:78060295-78060345	Hepatocyte	liver:	n/a
15	chr15:78077656-78077706	AG04450	lung:	fetal
16	chr15:78060295-78060345	PANC-1	pancreas:	n/a
17	chr15:78077656-78077706	AG04449	skin:	fetal
18	chr15:78077656-78077706	Caco-2	colon:	n/a
19	chr15:78077656-78077706	SK-N-SH_RA	brain:	n/a
20	chr15:78077656-78077706	PANC-1	pancreas:	n/a
21	chr15:78060295-78060345	HL-60	blood:	n/a
22	chr15:78103228-78103278	BE2_C	brain:	n/a
23	chr15:78060295-78060345	RPTEC	kidney:	n/a
24	chr15:78077656-78077706	RPTEC	kidney:	n/a
25	chr15:78060295-78060345	Caco-2	colon:	n/a
26	chr15:78077656-78077706	GM19239	blood:	n/a
27	chr15:78103228-78103278	A549	lung:	n/a
28	chr15:78060295-78060345	HUVEC	blood vessel:	n/a
29	chr15:78077656-78077706	A549	lung:	n/a
30	chr15:78060295-78060345	AG04450	lung:	fetal
31	chr15:78103228-78103278	HUVEC	blood vessel:	n/a
32	chr15:78103228-78103278	HepG2	liver:	n/a
33	chr15:78103228-78103278	GM12892	blood:	n/a
34	chr15:78103228-78103278	HNPCEpiC	eye:	n/a
35	chr15:78077656-78077706	HPAEpiC	pulmonary alveolar:	n/a
36	chr15:78103228-78103278	HRCEpiC	kidney:	n/a
37	chr15:78060295-78060345	GM06990	blood:	n/a
38	chr15:78060295-78060345	SAEC	small airway:	n/a
39	chr15:78077656-78077706	HRPEpiC	eye:	n/a
40	chr15:78060295-78060345	BE2_C	brain:	n/a
41	chr15:78077656-78077706	BE2_C	brain:	n/a
42	chr15:78103228-78103278	MCF-7	breast:	n/a
43	chr15:78060295-78060345	HepG2	liver:	n/a
44	chr15:78077656-78077706	GM12878	blood:	n/a
45	chr15:78060295-78060345	ovcar-3	ovarian:	n/a
46	chr15:78060295-78060345	MCF10A-Er-Src	breast:	n/a
47	chr15:78103228-78103278	HCM	heart:	n/a
48	chr15:78060295-78060345	GM12892	blood:	n/a
49	chr15:78060295-78060345	ECC-1	luminal epithelium:	n/a
50	chr15:78077656-78077706	AG09319	gingival:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:78004582..78006437-chr15:78057929..78059969,2	MCF-7	breast:
2	chr15:77951754..77952701-chr15:78076956..78077942,7	K562	blood:
3	chr15:77925491..77927003-chr15:78065547..78066951,12	MCF-7	breast:
4	chr15:78086471..78089118-chr20:52208956..52211312,2	MCF-7	breast:
5	chr15:78097066..78100710-chr15:78102142..78106147,5	K562	blood:
6	chr15:78097737..78099826-chr15:78103179..78105100,2	MCF-7	breast:
7	chr15:78049309..78052245-chr15:78054880..78058301,3	K562	blood:
8	chr15:78097465..78099114-chr15:78102921..78104806,2	K562	blood:
9	chr15:78103078..78104823-chr15:78106896..78108558,2	K562	blood:
10	chr15:77925509..77926398-chr15:78076937..78077835,4	K562	blood:
11	chr15:78099210..78100960-chr15:78102155..78104684,2	K562	blood:
12	chr15:78059582..78063718-chr15:78064964..78067132,3	K562	blood:
13	chr15:77917906..77920772-chr15:78100061..78102458,2	K562	blood:
14	chr15:78041656..78043427-chr15:78100097..78102130,2	MCF-7	breast:
15	chr15:78029999..78032267-chr15:78076792..78079270,2	MCF-7	breast:
16	chr15:78083797..78085667-chr15:78106019..78108853,2	K562	blood:
17	chr15:78097465..78099114-chr15:78102921..78104806,2	K562	blood:
18	chr15:78079574..78081366-chr15:78081562..78083403,2	MCF-7	breast:
19	chr15:78099210..78100960-chr15:78102155..78104684,2	K562	blood:
20	chr15:78066595..78068537-chr15:78076215..78077798,2	K562	blood:
21	chr15:78092486..78095378-chr15:78106571..78109428,2	K562	blood:
22	chr15:78097066..78100710-chr15:78102142..78106147,5	K562	blood:
23	chr15:78088888..78092011-chr15:78092368..78096073,3	K562	blood:
24	chr15:78088888..78092011-chr15:78092368..78096073,3	K562	blood:
25	chr15:78064180..78065710-chr15:78076746..78078989,2	K562	blood:
26	chr15:78044160..78046640-chr15:78075370..78077627,2	K562	blood:
27	chr15:78059582..78063718-chr15:78064964..78067132,3	K562	blood:
28	chr15:78066595..78068537-chr15:78076215..78077798,2	K562	blood:
29	chr15:78083797..78085667-chr15:78106019..78108853,2	K562	blood:
30	chr15:78062199..78064857-chr15:78066773..78068430,2	K562	blood:
31	chr15:77948459..77951097-chr15:78104975..78107913,2	MCF-7	breast:
32	chr15:77951783..77952314-chr15:78066187..78066759,2	MCF-7	breast:
33	chr15:78097737..78099826-chr15:78103179..78105100,2	MCF-7	breast:
34	chr15:78045800..78048382-chr15:78053626..78056901,3	K562	blood:
35	chr15:78093726..78095482-chr15:78109302..78111368,2	K562	blood:
36	chr15:78062199..78064857-chr15:78066773..78068430,2	K562	blood:
37	chr15:77951815..77952789-chr15:78075941..78076556,2	K562	blood:
38	chr15:78064180..78065710-chr15:78076746..78078989,2	K562	blood:
39	chr15:77925532..77926425-chr15:78076783..78078398,4	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SH2D7-5	chr15:78080723-78081016	ENSG00000259213.1
2	lnc-SH2D7-5	chr15:78080231-78080917	ENSG00000259213.1
3	lnc-SH2D7-5	chr15:78079535-78079589	ENSG00000259213.1
4	lnc-SH2D7-5	chr15:78080414-78080487	ENSG00000259213.1
5	lnc-SH2D7-5	chr15:78079529-78079589	XLOC_011317
6	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047459
7	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047458
8	lnc-TBC1D2B-7	chr15:78088281-78088395	NONHSAT047460
9	lnc-SH2D7-5	chr15:78080231-78081011	XLOC_011317

No data

Variant related genes	Relation type
ENSG00000259213	TF binding region
LINGO1	TF binding region
ENSG00000259213	CpG island
LINGO1	CpG island
ENSG00000171940	chromatin interactions
ENSG00000259281	chromatin interactions
ENSG00000169783	chromatin interactions
ENSG00000259213	chromatin interactions

Extended variants
information (count: 2081 )
Associated
traits (count: 51 )

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	rs11635700	chr15:78055479-78055480	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs142736557	chr15:78055488-78055489	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs189733486	chr15:78055495-78055496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180872718	chr15:78055514-78055515	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs56013767	chr15:78055558-78055559	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs74027314	chr15:78055576-78055577	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs544914352	chr15:78055593-78055594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs560058428	chr15:78055594-78055595	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534177073	chr15:78055607-78055608	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs527580418	chr15:78055627-78055628	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs371462612	chr15:78055636-78055637	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs564991729	chr15:78055645-78055646	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs117003208	chr15:78055674-78055675	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs11630990	chr15:78055678-78055679	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs12908030	chr15:78055692-78055693	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs549584158	chr15:78055750-78055751	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs117637710	chr15:78055838-78055839	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs533400128	chr15:78055848-78055849	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs183493992	chr15:78055862-78055863	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs568513553	chr15:78055874-78055875	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs150187489	chr15:78055876-78055877	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs536430529	chr15:78055892-78055893	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs538783109	chr15:78055935-78055936	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs534479833	chr15:78055985-78055986	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs77976640	chr15:78055996-78055997	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs556745966	chr15:78056032-78056033	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs567521753	chr15:78056066-78056067	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs34271163	chr15:78056083-78056084	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs35405416	chr15:78056085-78056086	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs188128419	chr15:78056110-78056111	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs556340006	chr15:78056141-78056142	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs11632255	chr15:78056143-78056144	Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs138842736	chr15:78056189-78056190	Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs553531890	chr15:78056205-78056206	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553841252	chr15:78056213-78056214	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558952025	chr15:78056243-78056244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs542479551	chr15:78056360-78056361	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs149375266	chr15:78056389-78056390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs531163072	chr15:78056446-78056447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572472479	chr15:78056462-78056463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs541303818	chr15:78056473-78056474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs564875886	chr15:78056486-78056487	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532223679	chr15:78056506-78056507	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs28368690	chr15:78056512-78056513	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs144812101	chr15:78056521-78056522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs28508300	chr15:78056523-78056524	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs182035799	chr15:78056728-78056729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs145209741	chr15:78056786-78056787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140038633	chr15:78056800-78056801	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs550791251	chr15:78056811-78056812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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

Chromatin state (count:361 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78054200-78057400	Enhancers	Fetal Brain Female	brain
2	chr15:78054600-78055600	Enhancers	Brain Germinal Matrix	brain
3	chr15:78054600-78056600	Enhancers	Fetal Brain Male	brain
4	chr15:78055400-78055800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:78055400-78056200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr15:78055400-78056400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
7	chr15:78055600-78056200	Bivalent Enhancer	Brain Germinal Matrix	brain
8	chr15:78055600-78056600	Enhancers	H1 Cell Line	embryonic stem cell
9	chr15:78055600-78057200	Enhancers	HepG2	liver
10	chr15:78055800-78056200	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr15:78055800-78056200	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr15:78055800-78056200	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr15:78055800-78056400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr15:78055800-78056400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:78056000-78056200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr15:78056000-78056600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr15:78056000-78056600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr15:78056200-78058800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr15:78056200-78059800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr15:78056200-78060000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr15:78056200-78060200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr15:78056200-78060200	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr15:78056400-78059800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
24	chr15:78056400-78060000	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr15:78056400-78060200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr15:78056600-78059800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
27	chr15:78056600-78060400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr15:78058800-78059000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr15:78059000-78059800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr15:78059800-78061000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr15:78059800-78061000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:78059800-78061200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr15:78059800-78061200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr15:78060000-78061000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr15:78060000-78061400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr15:78060200-78061000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr15:78060200-78061000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr15:78060200-78061400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr15:78060200-78061800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr15:78060400-78061400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr15:78061000-78061200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr15:78061000-78061400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
43	chr15:78061000-78061800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr15:78061200-78062000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr15:78061600-78062000	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
46	chr15:78061800-78062000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr15:78061800-78074800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr15:78062000-78062200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr15:78062200-78068000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr15:78063000-78064600	Enhancers	Spleen	Spleen

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