Variant report

Variant	rs12912192
Chromosome Location	chr15:51057181-51057182
allele	A/G
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	NFIC	chr15:51056787-51057330	GM12878	blood:	n/a	n/a
2	ESR1	chr15:51057124-51057547	T-47D	breast:	n/a	chr15:51057366-51057381 chr15:51057365-51057382
3	POLR2A	chr15:51057143-51058131	SK-N-MC	brain:	n/a	n/a
4	TEAD4	chr15:51057113-51057610	HepG2	liver:	n/a	n/a
5	CEBPB	chr15:51056868-51057622	K562	blood:	n/a	n/a
6	POLR2A	chr15:51057112-51058590	Hela-S3	cervix:	n/a	n/a
7	TAF1	chr15:51057105-51058229	A549	lung:	n/a	n/a
8	TAF1	chr15:51057133-51058176	K562	blood:	n/a	n/a
9	CHD1	chr15:51056442-51058202	GM12878	blood:	n/a	n/a
10	RELA	chr15:51056535-51058305	GM12878	blood:	n/a	chr15:51057932-51057941 chr15:51057932-51057941
11	POLR2A	chr15:51056647-51058461	GM12878	blood:	n/a	n/a
12	ELF1	chr15:51056417-51058579	MCF-7	breast:	n/a	chr15:51057901-51057912 chr15:51057612-51057624 chr15:51057882-51057894
13	POLR2A	chr15:51057170-51058791	HepG2	liver:	n/a	n/a
14	POLR2A	chr15:51057126-51058381	IMR90	lung:	n/a	n/a
15	RUNX3	chr15:51057074-51058397	GM12878	blood:	n/a	n/a
16	HDAC2	chr15:51057057-51058393	MCF-7	breast:	n/a	chr15:51057256-51057270 chr15:51057258-51057272 chr15:51057261-51057275 chr15:51057260-51057274
17	TCF7L2	chr15:51057055-51057457	HepG2	liver:	n/a	chr15:51057387-51057401
18	HEY1	chr15:51057109-51058364	K562	blood:	n/a	chr15:51057799-51057814
19	EP300	chr15:51056616-51058369	GM12878	blood:	n/a	chr15:51056848-51056862 chr15:51057901-51057910 chr15:51057619-51057635 chr15:51057810-51057826
20	NFIC	chr15:51057048-51058216	GM12878	blood:	n/a	n/a
21	TBP	chr15:51056424-51058348	GM12878	blood:	n/a	n/a
22	STAT3	chr15:51056628-51057475	MCF10A-Er-Src	breast:	n/a	chr15:51056853-51056864
23	ETS1	chr15:51057181-51058152	A549	lung:	n/a	chr15:51057908-51057917 chr15:51057904-51057915 chr15:51058038-51058047 chr15:51057901-51057908
24	POLR2A	chr15:51057041-51058293	HUVEC	blood vessel:	n/a	n/a
25	PML	chr15:51056930-51058152	K562	blood:	n/a	n/a
26	CEBPB	chr15:51057145-51057655	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr15:51057168-51057631	A549	lung:	n/a	n/a
28	POLR2A	chr15:51056804-51058368	K562	blood:	n/a	n/a
29	TAF1	chr15:51057077-51057599	PFSK-1	brain:	n/a	n/a
30	POLR2A	chr15:51057096-51058224	HUVEC	blood vessel:	n/a	n/a
31	POLR2A	chr15:51057143-51058213	HepG2	liver:	n/a	n/a
32	TEAD4	chr15:51056725-51058345	K562	blood:	n/a	n/a
33	TCF7L2	chr15:51057162-51058163	HCT-116	colon:	n/a	chr15:51057387-51057401
34	TCF7L2	chr15:51057121-51058414	Hela-S3	cervix:	n/a	chr15:51057387-51057401
35	ZNF384	chr15:51056669-51058178	K562	blood:	n/a	n/a
36	TBL1XR1	chr15:51056708-51057448	K562	blood:	n/a	n/a
37	POLR2A	chr15:51056416-51058453	K562	blood:	n/a	n/a
38	EBF1	chr15:51057180-51057277	GM12878	blood:	n/a	n/a
39	MAX	chr15:51056625-51058373	Hela-S3	cervix:	n/a	n/a
40	IRF1	chr15:51056538-51058325	K562	blood:	n/a	chr15:51057647-51057661 chr15:51056849-51056863 chr15:51057026-51057037 chr15:51056850-51056864 chr15:51056853-51056864 chr15:51057615-51057629 chr15:51057026-51057040 chr15:51056853-51056863 chr15:51057025-51057037 chr15:51056845-51056865 chr15:51057026-51057036 chr15:51056851-51056864 chr15:51057025-51057037
41	RELA	chr15:51056660-51058466	GM15510	blood:	n/a	chr15:51057932-51057941 chr15:51057932-51057941
42	POLR2A	chr15:51057102-51058480	Hela-S3	cervix:	n/a	n/a
43	MAX	chr15:51057011-51058444	A549	lung:	n/a	n/a
44	EP300	chr15:51057159-51058330	SK-N-SH	brain:	n/a	chr15:51057901-51057910 chr15:51057619-51057635 chr15:51057810-51057826
45	CUX1	chr15:51056509-51057271	GM12878	blood:	n/a	n/a
46	POLR2A	chr15:51056615-51058386	HepG2	liver:	n/a	n/a
47	MAZ	chr15:51056642-51058211	GM12878	blood:	n/a	n/a
48	MXI1	chr15:51057150-51058222	HepG2	liver:	n/a	n/a
49	UBTF	chr15:51057152-51058226	K562	blood:	n/a	n/a
50	CBX3	chr15:51057024-51058404	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:51056915..51057558-chr15:51070113..51070977,2	MCF-7	breast:
2	chr15:51056442..51059084-chr15:51199726..51202707,2	MCF-7	breast:
3	chr15:50982269..50983138-chr15:51056900..51057705,4	MCF-7	breast:
4	chr15:51056859..51057885-chr15:51146594..51147514,6	MCF-7	breast:
5	chr15:51056930..51057470-chr15:51070200..51070963,2	MCF-7	breast:
6	chr15:51056750..51061263-chr15:51087602..51092500,6	MCF-7	breast:
7	chr15:50976295..50981465-chr15:51052766..51059546,15	MCF-7	breast:
8	chr11:60926802..60929238-chr15:51056528..51059041,2	MCF-7	breast:
9	chr15:50982278..50983197-chr15:51056944..51057802,4	MCF-7	breast:
10	chr15:51039545..51042117-chr15:51054834..51058033,5	MCF-7	breast:
11	chr15:50977709..50979057-chr15:51056941..51058049,3	MCF-7	breast:
12	chr15:50977419..50980911-chr15:51055926..51058477,4	K562	blood:
13	chr15:51055767..51057855-chr19:39899197..39901640,2	MCF-7	breast:
14	chr15:51056515..51059362-chr15:51088829..51092887,6	MCF-7	breast:
15	chr15:50977319..50980700-chr15:51053372..51060901,7	MCF-7	breast:
16	chr15:51056915..51057629-chr15:51070050..51070613,2	MCF-7	breast:

Variant related genes	Relation type
SPPL2A	TF binding region
ENSG00000167987	Chromatin interaction
ENSG00000138600	Chromatin interaction
ENSG00000266559	Chromatin interaction
ENSG00000081014	Chromatin interaction
ENSG00000241130	Chromatin interaction
ENSG00000092439	Chromatin interaction
ENSG00000243027	Chromatin interaction

Extended variants
information (count: 73 )
Associated
traits (count: 5 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10519284	0.82[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap]
rs1052459	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs11635825	0.82[CHB][hapmap];1.00[CHD][hapmap];0.94[JPT][hapmap];0.89[TSI][hapmap]
rs11854949	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs12898588	0.82[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap]
rs12899074	0.82[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap]
rs12899321	0.82[ASN][1000 genomes]
rs12899700	0.82[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap]
rs12900933	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12902399	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12904353	1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs12905120	0.92[JPT][hapmap]
rs12906219	0.86[AMR][1000 genomes]
rs12906675	0.94[JPT][hapmap]
rs12907387	1.00[JPT][hapmap]
rs12907472	0.82[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap]
rs12907922	0.82[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap]
rs12908546	0.80[JPT][hapmap]
rs12911654	0.86[JPT][hapmap]
rs12911753	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs12913081	0.82[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap]
rs12913657	0.89[EUR][1000 genomes]
rs12914606	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12915607	0.94[AFR][1000 genomes]
rs12916113	0.93[JPT][hapmap]
rs12916510	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs12917408	0.82[LWK][hapmap];1.00[YRI][hapmap]
rs12917462	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16973487	0.82[CHB][hapmap];0.93[JPT][hapmap]
rs2304440	1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs2928138	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs35597009	0.84[ASN][1000 genomes]
rs485324	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs531366	0.82[CHB][hapmap];0.93[JPT][hapmap]
rs540257	0.82[CHB][hapmap];0.93[JPT][hapmap]
rs543821	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs615835	0.82[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap]
rs623639	0.82[CHB][hapmap];0.83[CHD][hapmap];0.94[JPT][hapmap]
rs623652	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs646856	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs7165492	0.82[CHB][hapmap];0.83[CHD][hapmap];1.00[JPT][hapmap]
rs7165684	0.93[JPT][hapmap]
rs7173321	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs8037161	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs8042919	0.94[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053966	chr15:50715572-51133186	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
2	nsv542383	chr15:50715572-51133186	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
3	nsv1043805	chr15:50715572-51208891	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv542384	chr15:50715572-51208891	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
5	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
6	nsv1051990	chr15:50745814-51133186	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv457134	chr15:50770868-51184583	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
8	nsv471242	chr15:50770868-51184583	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
9	nsv569396	chr15:50770868-51184583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
10	nsv457135	chr15:50770868-51189707	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
11	nsv569397	chr15:50770868-51189707	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
12	nsv1048621	chr15:50775451-51115535	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
13	nsv1047039	chr15:50782070-51187804	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
14	nsv542385	chr15:50782070-51187804	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
15	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
16	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
17	nsv1036081	chr15:50818569-51097229	Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
18	nsv1055112	chr15:50822035-51133186	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
19	nsv1042372	chr15:50846461-51208891	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
20	nsv542386	chr15:50846461-51208891	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
21	nsv569399	chr15:50874964-51562198	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
22	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
23	nsv904212	chr15:50979738-51132170	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
24	nsv904213	chr15:51011402-51119731	Strong transcription Weak transcription Flanking Active TSS Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
25	nsv1044320	chr15:51016364-51074061	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
26	nsv457137	chr15:51019117-51117524	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
27	nsv569402	chr15:51019117-51117524	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
28	nsv529339	chr15:51048579-51270372	Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

mRNA abundance (count:5)

SNP	Gene	Cis/trans	Tissue	Source
rs12912192	TRPM7	cis	cerebellum	SCAN
rs12912192	SPPL2A	cis	multi-tissue	Pritchard
rs12912192	SPATA5L1	cis	parietal	SCAN
rs12912192	SPPL2A	cis	cerebellum	SCAN
rs12912192	SPPL2A	cis	parietal	SCAN

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51046600-51057200	Weak transcription	Gastric	stomach
2	chr15:51053600-51057200	Weak transcription	Spleen	Spleen
3	chr15:51054800-51058000	Active TSS	Skeletal Muscle Male	skeletal muscle
4	chr15:51054800-51058200	Active TSS	Skeletal Muscle Female	skeletal muscle
5	chr15:51055200-51057200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr15:51055400-51058200	Active TSS	Right Ventricle	heart
7	chr15:51055600-51058000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
8	chr15:51055800-51058000	Active TSS	K562	blood
9	chr15:51055800-51058200	Active TSS	GM12878-XiMat	blood
10	chr15:51056000-51057200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:51056000-51058000	Active TSS	NHLF	lung
12	chr15:51056000-51058200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr15:51056000-51058200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr15:51056000-51058200	Active TSS	HSMM	muscle
15	chr15:51056000-51058200	Active TSS	HSMMtube	muscle
16	chr15:51056000-51058600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr15:51056000-51058600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr15:51056200-51057200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr15:51056200-51057400	Flanking Active TSS	Primary B cells from cord blood	blood
20	chr15:51056200-51057600	Active TSS	Right Atrium	heart
21	chr15:51056200-51057800	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
22	chr15:51056200-51058000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
23	chr15:51056200-51058000	Active TSS	Muscle Satellite Cultured Cells	--
24	chr15:51056200-51058000	Active TSS	Stomach Smooth Muscle	stomach
25	chr15:51056200-51058200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr15:51056200-51058200	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr15:51056200-51058200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr15:51056200-51058200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr15:51056200-51058200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
30	chr15:51056200-51058200	Active TSS	NH-A	brain
31	chr15:51056200-51058400	Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr15:51056200-51058400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr15:51056200-51058400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr15:51056200-51058400	Active TSS	Pancreatic Islets	Pancreatic Islet
35	chr15:51056200-51058600	Active TSS	Psoas Muscle	Psoas
36	chr15:51056400-51057200	Flanking Active TSS	Primary hematopoietic stem cells	blood
37	chr15:51056400-51057400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr15:51056400-51058000	Active TSS	Breast Myoepithelial Primary Cells	Breast
39	chr15:51056400-51058000	Active TSS	Primary T cells fromperipheralblood	blood
40	chr15:51056400-51058000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
41	chr15:51056400-51058000	Active TSS	HepG2	liver
42	chr15:51056400-51058000	Active TSS	HMEC	breast
43	chr15:51056400-51058000	Active TSS	NHEK	skin
44	chr15:51056400-51058200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
45	chr15:51056400-51058200	Active TSS	H1 Cell Line	embryonic stem cell
46	chr15:51056400-51058200	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr15:51056400-51058200	Active TSS	Primary T helper cells PMA-I stimulated	--
48	chr15:51056400-51058200	Active TSS	Brain Germinal Matrix	brain
49	chr15:51056400-51058200	Active TSS	Colonic Mucosa	Colon
50	chr15:51056400-51058200	Active TSS	Fetal Brain Male	brain

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