Variant report

Variant	rs8037013
Chromosome Location	chr15:50978023-50978024
allele	A/T
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	SIN3AK20	chr15:50977466-50980443	MCF-7	breast:	n/a	n/a
2	RCOR1	chr15:50977930-50980006	K562	blood:	n/a	n/a
3	POLR2A	chr15:50978003-50979732	H1-hESC	embryonic stem cell:	n/a	n/a
4	RELA	chr15:50977926-50979599	GM12891	blood:	n/a	n/a
5	SIN3A	chr15:50978011-50979654	GM12878	blood:	n/a	chr15:50979045-50979054 chr15:50978996-50979005
6	SIN3AK20	chr15:50977698-50979682	MCF-7	breast:	n/a	n/a
7	MTA3	chr15:50977773-50980208	GM12878	blood:	n/a	n/a
8	JUN	chr15:50977937-50980506	K562	blood:	n/a	n/a
9	GTF2F1	chr15:50978022-50979575	Hela-S3	cervix:	n/a	n/a
10	E2F6	chr15:50978002-50979558	H1-hESC	embryonic stem cell:	n/a	chr15:50978960-50978969 chr15:50979100-50979109 chr15:50979052-50979066
11	MAX	chr15:50977771-50979899	A549	lung:	n/a	chr15:50979048-50979064 chr15:50977886-50977895 chr15:50978996-50979005
12	KAP1	chr15:50978014-50980007	HEK293	kidney:	n/a	n/a
13	MAZ	chr15:50977853-50979700	GM12878	blood:	n/a	chr15:50979048-50979064 chr15:50977886-50977895 chr15:50978996-50979005
14	POLR2A	chr15:50977766-50979622	K562	blood:	n/a	n/a
15	MXI1	chr15:50977709-50979675	IMR90	lung:	n/a	chr15:50979045-50979054
16	MAX	chr15:50977901-50979675	MCF-7	breast:	n/a	chr15:50979048-50979064 chr15:50978996-50979005
17	EP300	chr15:50977900-50979732	GM12878	blood:	n/a	chr15:50978215-50978225 chr15:50979598-50979606 chr15:50978184-50978193 chr15:50978960-50978969 chr15:50979096-50979112
18	CTCF	chr15:50977980-50978130	MCF-7	breast:	n/a	n/a
19	POLR2A	chr15:50977911-50979627	GM12892	blood:	n/a	n/a
20	RAD21	chr15:50977709-50978087	HepG2	liver:	n/a	n/a
21	BHLHE40	chr15:50977862-50979784	GM12878	blood:	n/a	chr15:50979045-50979054 chr15:50979044-50979057 chr15:50978822-50978838 chr15:50979046-50979055 chr15:50978960-50978976
22	TBL1XR1	chr15:50977858-50978408	K562	blood:	n/a	n/a
23	WRNIP1	chr15:50977864-50979542	GM12878	blood:	n/a	n/a
24	PML	chr15:50977981-50979443	MCF-7	breast:	n/a	n/a
25	ZNF263	chr15:50977607-50979582	HEK293-T-REx	kidney:	n/a	chr15:50978773-50978782 chr15:50978770-50978779
26	ELF1	chr15:50977961-50979589	MCF-7	breast:	n/a	chr15:50978963-50978975 chr15:50978827-50978839 chr15:50978967-50978976 chr15:50978815-50978827
27	MAZ	chr15:50977906-50979555	K562	blood:	n/a	chr15:50979048-50979064 chr15:50978996-50979005
28	HA-E2F1	chr15:50978014-50979547	MCF-7	breast:	n/a	chr15:50978960-50978969 chr15:50979100-50979109 chr15:50979052-50979066
29	POLR2A	chr15:50977961-50979841	GM12878	blood:	n/a	n/a
30	TCF12	chr15:50977996-50979749	A549	lung:	n/a	chr15:50979073-50979081 chr15:50977998-50978005
31	HCFC1	chr15:50977853-50980080	Hela-S3	cervix:	n/a	n/a
32	MXI1	chr15:50977692-50980299	SK-N-SH	brain:	n/a	chr15:50979045-50979054
33	SRF	chr15:50977733-50979747	MCF-7	breast:	n/a	n/a
34	POLR2A	chr15:50977860-50980079	GM12891	blood:	n/a	n/a
35	POLR2A	chr15:50977928-50979620	GM12878	blood:	n/a	n/a
36	SIN3A	chr15:50977920-50979339	H1-hESC	embryonic stem cell:	n/a	chr15:50979045-50979054 chr15:50978996-50979005
37	POLR2A	chr15:50978000-50979633	PBDE	blood:	n/a	n/a
38	ELF1	chr15:50977754-50979567	MCF-7	breast:	n/a	chr15:50978963-50978975 chr15:50978827-50978839 chr15:50978967-50978976 chr15:50978815-50978827
39	POLR2A	chr15:50978004-50979975	K562	blood:	n/a	n/a
40	GATA2	chr15:50977947-50979478	SH-SY5Y	brain:	n/a	chr15:50978324-50978333 chr15:50978323-50978333 chr15:50978325-50978342 chr15:50978324-50978331 chr15:50978322-50978334

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	chr15:50977199..50979864-chr15:51198670..51201821,3	K562	blood:
7	chr15:50977319..50980700-chr15:51053372..51060901,7	MCF-7	breast:
8	chr15:50977014..50979307-chr16:3505643..3508008,2	MCF-7	breast:
9	chr15:50976192..50979125-chr15:51038150..51041035,2	K562	blood:
10	chr15:50976295..50981465-chr15:51052766..51059546,15	MCF-7	breast:
11	chr15:50977709..50979057-chr15:51056941..51058049,3	MCF-7	breast:
12	chr15:50977395..50978757-chr15:51177504..51178749,6	MCF-7	breast:
13	chr15:50645819..50647987-chr15:50977616..50981646,3	MCF-7	breast:
14	chr15:50645260..50648664-chr15:50977679..50981268,7	MCF-7	breast:
15	chr15:50977199..50981459-chr15:51198510..51202863,6	K562	blood:
16	chr15:50977048..50978856-chr15:51005682..51008712,3	K562	blood:
17	chr15:50977757..50980171-chr22:36876614..36879193,2	MCF-7	breast:
18	chr15:50977444..50978309-chr15:51200341..51200971,2	MCF-7	breast:

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

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs2414064	0.87[AFR][1000 genomes]
rs28439615	1.00[AMR][1000 genomes]
rs28483419	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28557300	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28692677	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28694689	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28789498	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28842528	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28890175	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59103950	1.00[AMR][1000 genomes]
rs7165257	1.00[AMR][1000 genomes]
rs7166172	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7166975	1.00[AMR][1000 genomes]
rs8033430	1.00[AMR][1000 genomes]
rs8036148	1.00[AMR][1000 genomes]
rs8036175	1.00[AMR][1000 genomes]
rs8039532	1.00[AMR][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	chr15:50976600-50978200	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr15:50976600-50978200	Flanking Active TSS	Liver	Liver
3	chr15:50976800-50978200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr15:50976800-50979800	Active TSS	Right Ventricle	heart
5	chr15:50977000-50979400	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr15:50977000-50979800	Active TSS	Breast Myoepithelial Primary Cells	Breast
7	chr15:50977000-50980200	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr15:50977000-50980400	Active TSS	GM12878-XiMat	blood
9	chr15:50977200-50978200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr15:50977200-50978200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr15:50977200-50978200	Flanking Active TSS	Dnd41	blood
12	chr15:50977200-50978400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
13	chr15:50977200-50978400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr15:50977200-50978400	Flanking Active TSS	HUVEC	blood vessel
15	chr15:50977200-50979200	Active TSS	H1 Cell Line	embryonic stem cell
16	chr15:50977200-50979200	Active TSS	Rectal Mucosa Donor 29	rectum
17	chr15:50977200-50979400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr15:50977200-50979400	Active TSS	K562	blood
19	chr15:50977200-50979800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr15:50977200-50979800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr15:50977200-50980000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr15:50977400-50978200	Flanking Active TSS	Brain Germinal Matrix	brain
23	chr15:50977400-50978400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
24	chr15:50977400-50978600	Active TSS	Right Atrium	heart
25	chr15:50977400-50978800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr15:50977400-50979200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr15:50977400-50979200	Active TSS	HMEC	breast
28	chr15:50977400-50979200	Active TSS	NHEK	skin
29	chr15:50977400-50979200	Active TSS	NHLF	lung
30	chr15:50977400-50979400	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr15:50977400-50979400	Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr15:50977400-50979400	Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr15:50977400-50979400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr15:50977400-50979400	Active TSS	HSMM	muscle
35	chr15:50977400-50979400	Active TSS	NHDF-Ad	bronchial
36	chr15:50977400-50979600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr15:50977400-50979600	Active TSS	HUES48 Cell Line	embryonic stem cell
38	chr15:50977400-50979600	Active TSS	Fetal Heart	heart
39	chr15:50977400-50979600	Active TSS	Left Ventricle	heart
40	chr15:50977400-50979800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chr15:50977400-50980400	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr15:50977600-50978200	Flanking Active TSS	Brain Hippocampus Middle	brain
43	chr15:50977600-50978200	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
44	chr15:50977600-50978200	Flanking Active TSS	Fetal Brain Female	brain
45	chr15:50977600-50978200	Flanking Active TSS	Placenta	Placenta
46	chr15:50977600-50978200	Flanking Active TSS	Hela-S3	cervix
47	chr15:50977600-50978400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr15:50977600-50978400	Flanking Active TSS	Primary T cells from cord blood	blood
49	chr15:50977600-50978400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr15:50977600-50978400	Flanking Active TSS	Adipose Nuclei	Adipose

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