Variant report

Variant	rs73397468
Chromosome Location	chr15:50978516-50978517
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	RFX5	chr15:50978153-50979761	Hela-S3	cervix:	n/a	n/a
2	MAX	chr15:50978075-50979750	MCF-7	breast:	n/a	chr15:50979048-50979064 chr15:50978996-50979005
3	MTA3	chr15:50978239-50979031	GM12878	blood:	n/a	n/a
4	E2F6	chr15:50978088-50979695	K562	blood:	n/a	chr15:50978960-50978969 chr15:50979100-50979109 chr15:50979052-50979066
5	POLR2A	chr15:50978379-50979713	PFSK-1	brain:	n/a	n/a
6	USF1	chr15:50978443-50979628	A549	lung:	n/a	chr15:50979044-50979055 chr15:50979045-50979054 chr15:50978995-50979006 chr15:50979044-50979057 chr15:50978822-50978838 chr15:50979046-50979055 chr15:50978960-50978976
7	RCOR1	chr15:50978234-50979543	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr15:50978162-50979277	K562	blood:	n/a	n/a
9	PAX5	chr15:50978290-50979472	GM12892	blood:	n/a	chr15:50979100-50979109 chr15:50978956-50978965 chr15:50979332-50979359 chr15:50979058-50979067
10	CHD2	chr15:50978300-50979648	H1-hESC	embryonic stem cell:	n/a	chr15:50978538-50978548
11	CHD1	chr15:50978222-50979500	GM12878	blood:	n/a	chr15:50978538-50978548
12	SIN3AK20	chr15:50977466-50980443	MCF-7	breast:	n/a	n/a
13	TAF1	chr15:50978329-50979326	H1-neurons	neurons:	n/a	n/a
14	MAX	chr15:50978284-50979601	HCT-116	colon:	n/a	chr15:50979048-50979064 chr15:50978996-50979005
15	POU2F2	chr15:50978182-50979416	GM12878	blood:	n/a	n/a
16	BHLHE40	chr15:50978197-50979635	HepG2	liver:	n/a	chr15:50979045-50979054 chr15:50979044-50979057 chr15:50978822-50978838 chr15:50979046-50979055 chr15:50978960-50978976
17	RCOR1	chr15:50977930-50980006	K562	blood:	n/a	n/a
18	ZEB1	chr15:50978169-50978771	GM12878	blood:	n/a	n/a
19	POLR2A	chr15:50978003-50979732	H1-hESC	embryonic stem cell:	n/a	n/a
20	RCOR1	chr15:50978229-50979740	GM12878	blood:	n/a	n/a
21	MAX	chr15:50978099-50979679	K562	blood:	n/a	chr15:50979048-50979064 chr15:50978996-50979005
22	E2F6	chr15:50978180-50979400	K562	blood:	n/a	chr15:50978960-50978969 chr15:50979100-50979109 chr15:50979052-50979066
23	POLR2A	chr15:50978169-50979455	H1-hESC	embryonic stem cell:	n/a	n/a
24	POLR2A	chr15:50978153-50979478	H1-neurons	neurons:	n/a	n/a
25	RELA	chr15:50977926-50979599	GM12891	blood:	n/a	n/a
26	TEAD4	chr15:50978471-50979556	ECC-1	luminal epithelium:	n/a	n/a
27	GABPA	chr15:50978229-50979001	A549	lung:	n/a	chr15:50978960-50978969
28	TBP	chr15:50978166-50979502	H1-hESC	embryonic stem cell:	n/a	n/a
29	SIN3A	chr15:50978011-50979654	GM12878	blood:	n/a	chr15:50979045-50979054 chr15:50978996-50979005
30	POLR2A	chr15:50978385-50979538	GM12878	blood:	n/a	n/a
31	CEBPB	chr15:50978256-50979686	Hela-S3	cervix:	n/a	chr15:50979356-50979373
32	MYC	chr15:50978315-50979536	Hela-S3	cervix:	n/a	chr15:50979048-50979064 chr15:50978996-50979005
33	TBL1XR1	chr15:50978408-50979701	GM12878	blood:	n/a	n/a
34	HMGN3	chr15:50978202-50979420	K562	blood:	n/a	chr15:50978325-50978332
35	E2F4	chr15:50978335-50979401	K562	blood:	n/a	chr15:50978960-50978969 chr15:50979100-50979109 chr15:50979052-50979066
36	TCF12	chr15:50978404-50979554	ECC-1	luminal epithelium:	n/a	chr15:50979073-50979081
37	ELF1	chr15:50978339-50979258	K562	blood:	n/a	chr15:50978963-50978975 chr15:50978827-50978839 chr15:50978967-50978976 chr15:50978815-50978827
38	SIN3AK20	chr15:50977698-50979682	MCF-7	breast:	n/a	n/a
39	TAF1	chr15:50978377-50979491	GM12878	blood:	n/a	n/a
40	MAX	chr15:50978069-50979672	HCT-116	colon:	n/a	chr15:50979048-50979064 chr15:50978996-50979005
41	E2F4	chr15:50978394-50979623	MCF10A-Er-Src	breast:	n/a	chr15:50978960-50978969 chr15:50979100-50979109 chr15:50979052-50979066
42	CTCF	chr15:50978203-50979373	GM12878	blood:	n/a	chr15:50978824-50978837
43	TAF1	chr15:50978259-50979505	H1-hESC	embryonic stem cell:	n/a	n/a
44	POLR2A	chr15:50978245-50979575	IMR90	lung:	n/a	n/a
45	JUND	chr15:50978225-50979497	A549	lung:	n/a	n/a
46	POLR2A	chr15:50978222-50979378	HEK293	kidney:	n/a	n/a
47	TAF1	chr15:50978281-50979451	HepG2	liver:	n/a	n/a
48	CTCF	chr15:50978380-50978530	GM12869	blood:	n/a	n/a
49	USF2	chr15:50978243-50979662	GM12878	blood:	n/a	chr15:50979045-50979054 chr15:50979044-50979057 chr15:50979044-50979055 chr15:50978822-50978838 chr15:50979046-50979055 chr15:50978996-50979007 chr15:50978960-50978976
50	MTA3	chr15:50977773-50980208	GM12878	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:50650545..50654228-chr15:50976566..50979826,3	MCF-7	breast:
2	chr15:50977313..50978812-chr15:51169055..51169789,4	MCF-7	breast:
3	chr15:50977419..50980911-chr15:51055926..51058477,4	K562	blood:
4	chr15:50977442..50979922-chr15:51198976..51201748,2	MCF-7	breast:
5	chr15:50977828..50980537-chr15:51197788..51202411,5	MCF-7	breast:
6	chr11:46368370..46369020-chr15:50978346..50979082,2	NB4	blood:
7	chr15:50977199..50979864-chr15:51198670..51201821,3	K562	blood:
8	chr15:50977319..50980700-chr15:51053372..51060901,7	MCF-7	breast:
9	chr15:50977014..50979307-chr16:3505643..3508008,2	MCF-7	breast:
10	chr15:50976192..50979125-chr15:51038150..51041035,2	K562	blood:
11	chr15:50978167..50979033-chr3:171757700..171758531,2	Hela-S3	cervix:
12	chr15:50976295..50981465-chr15:51052766..51059546,15	MCF-7	breast:
13	chr15:50977709..50979057-chr15:51056941..51058049,3	MCF-7	breast:
14	chr1:185286540..185287260-chr15:50978376..50979105,2	Hela-S3	cervix:
15	chr15:50977395..50978757-chr15:51177504..51178749,6	MCF-7	breast:
16	chr15:50645819..50647987-chr15:50977616..50981646,3	MCF-7	breast:
17	chr1:174968276..174969269-chr15:50978167..50978813,2	Hela-S3	cervix:
18	chr15:50645260..50648664-chr15:50977679..50981268,7	MCF-7	breast:
19	chr15:50977199..50981459-chr15:51198510..51202863,6	K562	blood:
20	chr15:50977048..50978856-chr15:51005682..51008712,3	K562	blood:
21	chr15:50977757..50980171-chr22:36876614..36879193,2	MCF-7	breast:

Variant related genes	Relation type
RN7SL354P	TF binding region
ENSG00000104064	Chromatin interaction
ENSG00000273004	Chromatin interaction
ENSG00000122390	Chromatin interaction
ENSG00000264109	Chromatin interaction
ENSG00000075420	Chromatin interaction
ENSG00000081014	Chromatin interaction
ENSG00000262621	Chromatin interaction
ENSG00000149091	Chromatin interaction
ENSG00000244879	Chromatin interaction
ENSG00000259715	Chromatin interaction
ENSG00000138600	Chromatin interaction
ENSG00000100348	Chromatin interaction
ENSG00000259773	Chromatin interaction
ENSG00000116161	Chromatin interaction

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs12101792	0.97[AFR][1000 genomes]
rs12102160	0.97[AFR][1000 genomes]
rs16963806	0.92[AFR][1000 genomes]
rs16963808	0.92[AFR][1000 genomes]
rs16963812	0.92[AFR][1000 genomes]
rs28422095	0.92[AFR][1000 genomes]
rs28452820	0.97[AFR][1000 genomes]
rs28464149	0.92[AFR][1000 genomes]
rs28478598	0.92[AFR][1000 genomes]
rs28504102	0.92[AFR][1000 genomes]
rs28575682	0.97[AFR][1000 genomes]
rs28613018	0.92[AFR][1000 genomes]
rs28699109	0.92[AFR][1000 genomes]
rs28763655	0.92[AFR][1000 genomes]
rs28806878	0.97[AFR][1000 genomes]
rs28828095	0.92[AFR][1000 genomes]
rs55996689	0.92[AFR][1000 genomes]
rs56277600	0.92[AFR][1000 genomes]
rs58579351	0.92[AFR][1000 genomes]
rs58700289	0.92[AFR][1000 genomes]
rs58899101	0.90[AFR][1000 genomes]
rs58959948	0.92[AFR][1000 genomes]
rs59036721	0.92[AFR][1000 genomes]
rs60192084	0.92[AFR][1000 genomes]
rs61216053	0.92[AFR][1000 genomes]
rs73395523	0.92[AFR][1000 genomes]
rs73395527	0.92[AFR][1000 genomes]
rs73395537	0.92[AFR][1000 genomes]
rs73395538	0.92[AFR][1000 genomes]
rs73395545	0.92[AFR][1000 genomes]
rs73395552	0.92[AFR][1000 genomes]
rs73395590	0.92[AFR][1000 genomes]
rs73397406	0.92[AFR][1000 genomes]
rs73397410	0.92[AFR][1000 genomes]
rs73397449	0.88[AFR][1000 genomes]
rs73397461	1.00[AFR][1000 genomes]
rs73397473	0.95[AFR][1000 genomes]
rs73408905	0.92[AFR][1000 genomes]
rs73408906	0.92[AFR][1000 genomes]
rs73408921	0.92[AFR][1000 genomes]
rs73408925	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045456	chr15:50592472-51019873	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv948579	chr15:50645530-51045564	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	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
8	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
9	nsv1054970	chr15:50761410-51036625	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers 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	32 gene(s)	inside rSNPs	diseases
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	nsv431389	chr15:50795835-50979738	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
21	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
22	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
23	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
24	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
25	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
26	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
27	nsv1051400	chr15:50890333-51046283	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50976800-50979800	Active TSS	Right Ventricle	heart
2	chr15:50977000-50979400	Active TSS	iPS-20b Cell Line	embryonic stem cell
3	chr15:50977000-50979800	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr15:50977000-50980200	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chr15:50977000-50980400	Active TSS	GM12878-XiMat	blood
6	chr15:50977200-50979200	Active TSS	H1 Cell Line	embryonic stem cell
7	chr15:50977200-50979200	Active TSS	Rectal Mucosa Donor 29	rectum
8	chr15:50977200-50979400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr15:50977200-50979400	Active TSS	K562	blood
10	chr15:50977200-50979800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr15:50977200-50979800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr15:50977200-50980000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr15:50977400-50978600	Active TSS	Right Atrium	heart
14	chr15:50977400-50978800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr15:50977400-50979200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr15:50977400-50979200	Active TSS	HMEC	breast
17	chr15:50977400-50979200	Active TSS	NHEK	skin
18	chr15:50977400-50979200	Active TSS	NHLF	lung
19	chr15:50977400-50979400	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr15:50977400-50979400	Active TSS	HUES64 Cell Line	embryonic stem cell
21	chr15:50977400-50979400	Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr15:50977400-50979400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr15:50977400-50979400	Active TSS	HSMM	muscle
24	chr15:50977400-50979400	Active TSS	NHDF-Ad	bronchial
25	chr15:50977400-50979600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr15:50977400-50979600	Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr15:50977400-50979600	Active TSS	Fetal Heart	heart
28	chr15:50977400-50979600	Active TSS	Left Ventricle	heart
29	chr15:50977400-50979800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
30	chr15:50977400-50980400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr15:50977600-50978600	Flanking Active TSS	Primary B cells from cord blood	blood
32	chr15:50977600-50978800	Flanking Active TSS	Primary hematopoietic stem cells	blood
33	chr15:50977600-50978800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
34	chr15:50977600-50979000	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
35	chr15:50977600-50979400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr15:50977600-50979400	Active TSS	Fetal Intestine Small	intestine
37	chr15:50977600-50979400	Active TSS	Fetal Kidney	kidney
38	chr15:50977600-50979400	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr15:50977600-50979600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr15:50977600-50979600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr15:50977600-50979600	Active TSS	Brain Angular Gyrus	brain
42	chr15:50977600-50979600	Active TSS	Fetal Intestine Large	intestine
43	chr15:50977600-50979800	Active TSS	H9 Cell Line	embryonic stem cell
44	chr15:50977600-50979800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr15:50977600-50980000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:50977600-50980000	Active TSS	HSMMtube	muscle
47	chr15:50977800-50979200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:50977800-50979200	Active TSS	Muscle Satellite Cultured Cells	--
49	chr15:50977800-50979200	Active TSS	Colonic Mucosa	Colon
50	chr15:50977800-50979200	Active TSS	Osteobl	bone

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