Variant report

Variant	esv1836748
Chromosome Location	chr15:78111223-78112524
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	BACH1	chr15:78111596-78111934	H1-hESC	embryonic stem cell:	n/a	n/a
2	CHD1	chr15:78111718-78111742	H1-hESC	embryonic stem cell:	n/a	n/a
3	CREB1	chr15:78112210-78112963	A549	lung:	n/a	n/a
4	CTBP2	chr15:78111581-78112011	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr15:78112509-78113097	MCF-7	breast:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781
6	CTCF	chr15:78112505-78112550	MCF-7	breast:	n/a	n/a
7	CTCF	chr15:78112512-78112875	H1-hESC	embryonic stem cell:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781
8	CTCF	chr15:78111763-78111842	GM12891	blood:	n/a	n/a
9	CTCF	chr15:78112465-78113115	HCT-116	colon:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781
10	CTCF	chr15:78112259-78112303	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr15:78112362-78114448	A549	lung:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781 chr15:78113982-78114000
12	CTCF	chr15:78112223-78114736	SK-N-SH	brain:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781 chr15:78113982-78114000
13	CTCF	chr15:78112511-78112987	K562	blood:	n/a	chr15:78112615-78112628 chr15:78112615-78112624 chr15:78112771-78112781
14	E2F6	chr15:78112416-78112950	A549	lung:	n/a	chr15:78112646-78112657 chr15:78112466-78112475
15	E2F6	chr15:78112134-78112855	H1-hESC	embryonic stem cell:	n/a	chr15:78112646-78112657 chr15:78112466-78112475
16	E2F6	chr15:78112308-78112963	K562	blood:	n/a	chr15:78112646-78112657 chr15:78112466-78112475
17	FOXP2	chr15:78111601-78111993	PFSK-1	brain:	n/a	n/a
18	FOXP2	chr15:78111679-78111938	SK-N-MC	brain:	n/a	n/a
19	GABPA	chr15:78111477-78111954	H1-hESC	embryonic stem cell:	n/a	n/a
20	GTF2F1	chr15:78112236-78112263	H1-hESC	embryonic stem cell:	n/a	n/a
21	HMGN3	chr15:78111664-78111678	K562	blood:	n/a	n/a
22	HMGN3	chr15:78112346-78112946	K562	blood:	n/a	n/a
23	MAX	chr15:78111546-78112036	H1-hESC	embryonic stem cell:	n/a	n/a
24	MAX	chr15:78111477-78113075	A549	lung:	n/a	n/a
25	MAX	chr15:78112127-78113107	H1-hESC	embryonic stem cell:	n/a	n/a
26	MAX	chr15:78112318-78112922	ECC-1	luminal epithelium:	n/a	n/a
27	MAX	chr15:78112425-78113011	A549	lung:	n/a	n/a
28	MAX	chr15:78111564-78112045	ECC-1	luminal epithelium:	n/a	n/a
29	MYC	chr15:78111684-78111871	MCF-7	breast:	n/a	n/a
30	NRF1	chr15:78111764-78111913	H1-hESC	embryonic stem cell:	n/a	n/a
31	PAX5	chr15:78111581-78111793	GM12892	blood:	n/a	n/a
32	POLR2A	chr15:78111574-78111639	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr15:78111480-78112107	PFSK-1	brain:	n/a	n/a
34	POLR2A	chr15:78111648-78111709	H1-hESC	embryonic stem cell:	n/a	n/a
35	POLR2A	chr15:78111682-78111865	MCF-7	breast:	n/a	n/a
36	POLR2A	chr15:78111620-78118444	SK-N-MC	brain:	n/a	n/a
37	POLR2A	chr15:78112194-78112776	H1-neurons	neurons:	n/a	n/a
38	POLR2A	chr15:78111455-78111921	ECC-1	luminal epithelium:	n/a	n/a
39	POLR2A	chr15:78111197-78112117	H1-neurons	neurons:	n/a	n/a
40	POLR2A	chr15:78111325-78112987	H1-neurons	neurons:	n/a	n/a
41	RAD21	chr15:78112503-78112941	MCF-7	breast:	n/a	chr15:78112772-78112782
42	RAD21	chr15:78112326-78113049	H1-hESC	embryonic stem cell:	n/a	chr15:78112772-78112782 chr15:78112433-78112445
43	RAD21	chr15:78112490-78112993	A549	lung:	n/a	chr15:78112772-78112782
44	RAD21	chr15:78112493-78112942	MCF-7	breast:	n/a	chr15:78112772-78112782
45	RAD21	chr15:78112385-78113087	SK-N-SH	brain:	n/a	chr15:78112772-78112782 chr15:78112433-78112445
46	RAD21	chr15:78112501-78113042	ECC-1	luminal epithelium:	n/a	chr15:78112772-78112782
47	REST	chr15:78112469-78112837	PFSK-1	brain:	n/a	n/a
48	REST	chr15:78111340-78112967	H1-neurons	neurons:	n/a	chr15:78111574-78111587 chr15:78111549-78111562 chr15:78111552-78111565 chr15:78111572-78111590 chr15:78111748-78111761 chr15:78111574-78111587
49	SIN3A	chr15:78112186-78112954	H1-hESC	embryonic stem cell:	n/a	chr15:78112779-78112790
50	TAF1	chr15:78111657-78112061	H1-neurons	neurons:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:78111390-78111440	HCPEpiC	choroid plexus:	n/a
2	chr15:78111390-78111440	HCPEpiC	choroid plexus:	n/a
3	chr15:78111196-78111246	HMEC	breast:	n/a
4	chr15:78112026-78112076	HMEC	breast:	n/a
5	chr15:78111196-78111246	SK-N-SH_RA	brain:	n/a
6	chr15:78111390-78111440	AG10803	skin:	n/a
7	chr15:78111390-78111440	SKMC	muscle:	n/a
8	chr15:78111196-78111246	ProgFib	skin:	n/a
9	chr15:78111390-78111440	HNPCEpiC	eye:	n/a
10	chr15:78111390-78111440	HMEC	breast:	n/a
11	chr15:78111390-78111440	RPTEC	kidney:	n/a
12	chr15:78111830-78111880	T-47D	breast:	n/a
13	chr15:78112026-78112076	HCM	heart:	n/a
14	chr15:78112026-78112076	HL-60	blood:	n/a
15	chr15:78112026-78112076	HCT-116	colon:	n/a
16	chr15:78111196-78111246	A549	lung:	n/a
17	chr15:78111830-78111880	Hepatocyte	liver:	n/a
18	chr15:78111196-78111246	HepG2	liver:	n/a
19	chr15:78111830-78111880	HRPEpiC	eye:	n/a
20	chr15:78111830-78111880	AG09319	gingival:	n/a
21	chr15:78112026-78112076	MCF10A-Er-Src	breast:	n/a
22	chr15:78112026-78112076	BJ	skin:	n/a
23	chr15:78112026-78112076	HepG2	liver:	n/a
24	chr15:78111830-78111880	ProgFib	skin:	n/a
25	chr15:78111196-78111246	SKMC	muscle:	n/a
26	chr15:78112026-78112076	HCPEpiC	choroid plexus:	n/a
27	chr15:78112026-78112076	AG04449	skin:	fetal
28	chr15:78111196-78111246	NHDF-neo	bronchial:	n/a
29	chr15:78112026-78112076	GM19239	blood:	n/a
30	chr15:78111830-78111880	IMR90	lung:	fetal
31	chr15:78112026-78112076	GM12878	blood:	n/a
32	chr15:78111830-78111880	NB4	blood:	n/a
33	chr15:78111196-78111246	GM19239	blood:	n/a
34	chr15:78111390-78111440	SAEC	small airway:	n/a
35	chr15:78111196-78111246	HPAEpiC	pulmonary alveolar:	n/a
36	chr15:78112026-78112076	U87	brain:	n/a
37	chr15:78111830-78111880	GM12878	blood:	n/a
38	chr15:78111390-78111440	Hela-S3	cervix:	n/a
39	chr15:78111196-78111246	NH-A	brain:	n/a
40	chr15:78111390-78111440	Jurkat	blood:	n/a
41	chr15:78111390-78111440	SK-N-SH	brain:	n/a
42	chr15:78111390-78111440	HCM	heart:	n/a
43	chr15:78111830-78111880	SAEC	small airway:	n/a
44	chr15:78112026-78112076	PANC-1	pancreas:	n/a
45	chr15:78111390-78111440	GM12878	blood:	n/a
46	chr15:78111390-78111440	AG04450	lung:	fetal
47	chr15:78111390-78111440	PrEC	prostate:	n/a
48	chr15:78111830-78111880	HCT-116	colon:	n/a
49	chr15:78111830-78111880	HIPEpiC	eye:	n/a
50	chr15:78111196-78111246	SK-N-MC	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:77925299..77927652-chr15:78112444..78114100,3	MCF-7	breast:
2	chr15:78109668..78112280-chr15:78112604..78115106,3	MCF-7	breast:
3	chr15:78093726..78095482-chr15:78109302..78111368,2	K562	blood:
4	chr15:77925397..77927315-chr15:78112259..78115116,2	K562	blood:
5	chr15:77925435..77927439-chr15:78112259..78115090,22	K562	blood:
6	chr15:77923251..77928296-chr15:78111448..78115771,8	MCF-7	breast:
7	chr15:77925397..77928069-chr15:78112259..78116246,3	K562	blood:
8	chr15:77925072..77927787-chr15:78111223..78115888,59	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TBC1D2B-7	chr15:78112376-78112566	NONHSAT047460
2	lnc-TBC1D2B-7	chr15:78111613-78111870	NONHSAT047458

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

Extended variants
information (count: 34 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:34 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs527646951	chr15:78111274-78111275	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs145382349	chr15:78111295-78111296	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs180908784	chr15:78111359-78111360	Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs35981882	chr15:78111402-78111403	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs372088592	chr15:78111519-78111520	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs12911998	chr15:78111563-78111564	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs531822614	chr15:78111598-78111599	Bivalent/Poised TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs550026719	chr15:78111630-78111631	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
9	rs571460945	chr15:78111643-78111644	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
10	rs185470896	chr15:78111669-78111670	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
11	rs372187360	chr15:78111723-78111724	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
12	rs553992491	chr15:78111743-78111744	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
13	rs561620983	chr15:78111787-78111788	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
14	rs189759565	chr15:78111797-78111798	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs565542642	chr15:78111824-78111825	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
16	rs536214865	chr15:78111874-78111875	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs554381935	chr15:78111882-78111883	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs143130993	chr15:78111915-78111916	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs113747076	chr15:78111924-78111925	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs575767569	chr15:78111929-78111930	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs7497690	chr15:78111981-78111982	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs543093259	chr15:78111999-78112000	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs55953854	chr15:78112058-78112059	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs577807521	chr15:78112143-78112144	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs7182763	chr15:78112151-78112152	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs560793934	chr15:78112184-78112185	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs534884837	chr15:78112228-78112229	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs572372510	chr15:78112232-78112233	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs56061966	chr15:78112233-78112234	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs550285306	chr15:78112234-78112235	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376544923	chr15:78112418-78112419	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs565081708	chr15:78112496-78112497	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs532287133	chr15:78112522-78112523	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs112033856	chr15:78112524-78112525	Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	2 gene(s)	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:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78107400-78111600	Weak transcription	Gastric	stomach
2	chr15:78109800-78111800	Bivalent Enhancer	Spleen	Spleen
3	chr15:78110600-78111600	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:78110600-78111600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
5	chr15:78110600-78111600	Bivalent Enhancer	Esophagus	oesophagus
6	chr15:78110600-78111600	Bivalent Enhancer	Fetal Muscle Leg	muscle
7	chr15:78110600-78111800	Bivalent Enhancer	Placenta	Placenta
8	chr15:78110600-78112800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
9	chr15:78110600-78112800	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
10	chr15:78110600-78113000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
11	chr15:78110600-78113000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
12	chr15:78110600-78113200	Active TSS	Brain Angular Gyrus	brain
13	chr15:78110800-78111400	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
14	chr15:78110800-78111400	Bivalent Enhancer	Fetal Brain Male	brain
15	chr15:78110800-78111600	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr15:78110800-78111600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr15:78110800-78111600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr15:78110800-78111600	Bivalent Enhancer	Colonic Mucosa	Colon
19	chr15:78110800-78111600	Bivalent/Poised TSS	Right Ventricle	heart
20	chr15:78110800-78111600	Bivalent Enhancer	HMEC	breast
21	chr15:78110800-78112800	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
22	chr15:78110800-78112800	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr15:78110800-78113000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr15:78111000-78111400	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
25	chr15:78111000-78111400	Bivalent Enhancer	Fetal Heart	heart
26	chr15:78111000-78111400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
27	chr15:78111000-78111600	Bivalent/Poised TSS	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr15:78111000-78111600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr15:78111000-78111600	Bivalent Enhancer	Lung	lung
30	chr15:78111000-78112600	Transcr. at gene 5' and 3'	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr15:78111000-78112600	Active TSS	Fetal Brain Female	brain
32	chr15:78111000-78112800	Active TSS	H9 Cell Line	embryonic stem cell
33	chr15:78111000-78112800	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
34	chr15:78111000-78112800	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
35	chr15:78111000-78112800	Bivalent/Poised TSS	Ovary	ovary
36	chr15:78111000-78113000	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
37	chr15:78111000-78113600	Active TSS	Brain Inferior Temporal Lobe	brain
38	chr15:78111200-78111400	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr15:78111200-78111400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr15:78111200-78111400	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr15:78111200-78111400	Flanking Bivalent TSS/Enh	Duodenum Smooth Muscle	Duodenum
42	chr15:78111200-78111400	Bivalent Enhancer	Fetal Stomach	stomach
43	chr15:78111200-78111400	Enhancers	Placenta Amnion	Placenta Amnion
44	chr15:78111200-78111400	Active TSS	Right Atrium	heart
45	chr15:78111200-78111400	Bivalent/Poised TSS	Small Intestine	intestine
46	chr15:78111200-78111600	Active TSS	Primary hematopoietic stem cells	blood
47	chr15:78111200-78111600	Enhancers	Pancreas	Pancrea
48	chr15:78111200-78112200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
49	chr15:78111200-78112600	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr15:78111200-78112600	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell

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