Variant report

Variant	rs72759077
Chromosome Location	chr5:42909034-42909035
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:129)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:129 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:42909031-42909314	LNCaP	prostate:	n/a	n/a
2	ZNF143	chr5:42908971-42909361	K562	blood:	n/a	n/a
3	NRF1	chr5:42908914-42909266	HepG2	liver:	n/a	chr5:42909110-42909121
4	MYC	chr5:42908648-42909398	K562	blood:	n/a	n/a
5	RAD21	chr5:42908868-42909520	HCT-116	colon:	n/a	n/a
6	EP300	chr5:42908995-42909265	GM12878	blood:	n/a	n/a
7	ZMIZ1	chr5:42908966-42909361	K562	blood:	n/a	n/a
8	RAD21	chr5:42908919-42909536	A549	lung:	n/a	n/a
9	RAD21	chr5:42908954-42909399	A549	lung:	n/a	n/a
10	RAD21	chr5:42908678-42909411	H1-hESC	embryonic stem cell:	n/a	n/a
11	MYBL2	chr5:42908712-42909252	HepG2	liver:	n/a	n/a
12	ARID3A	chr5:42908844-42909308	K562	blood:	n/a	n/a
13	PML	chr5:42908704-42909330	GM12878	blood:	n/a	n/a
14	CTCF	chr5:42908960-42909321	HepG2	liver:	n/a	n/a
15	YY1	chr5:42908969-42909321	GM12878	blood:	n/a	n/a
16	GTF2F1	chr5:42909024-42909386	Hela-S3	cervix:	n/a	n/a
17	MTA3	chr5:42908539-42909442	GM12878	blood:	n/a	n/a
18	CTCF	chr5:42908925-42909387	K562	blood:	n/a	n/a
19	CTCF	chr5:42908975-42909361	A549	lung:	n/a	n/a
20	POLR2A	chr5:42908847-42909334	PANC-1	pancreas:	n/a	n/a
21	POLR2A	chr5:42908699-42909221	MCF10A-Er-Src	breast:	n/a	n/a
22	CTCF	chr5:42909027-42909308	HUVEC	blood vessel:	n/a	n/a
23	PAX5	chr5:42909012-42909339	GM12878	blood:	n/a	n/a
24	CTCF	chr5:42909021-42909339	A549	lung:	n/a	n/a
25	RAD21	chr5:42908997-42909436	HepG2	liver:	n/a	n/a
26	CHD2	chr5:42908975-42909339	GM12878	blood:	n/a	n/a
27	CTCF	chr5:42908941-42909384	H1-hESC	embryonic stem cell:	n/a	n/a
28	MAX	chr5:42908777-42909306	Hela-S3	cervix:	n/a	n/a
29	RAD21	chr5:42908679-42909502	IMR90	lung:	n/a	n/a
30	CTCF	chr5:42909032-42909300	Pancreas_OC	pancreas:	n/a	n/a
31	WRNIP1	chr5:42908950-42909362	GM12878	blood:	n/a	n/a
32	TEAD4	chr5:42908890-42909278	HepG2	liver:	n/a	n/a
33	RCOR1	chr5:42908679-42909352	K562	blood:	n/a	n/a
34	CTCF	chr5:42909017-42909338	GM12878	blood:	n/a	n/a
35	MAX	chr5:42908671-42909297	H1-hESC	embryonic stem cell:	n/a	n/a
36	RAD21	chr5:42908976-42909384	MCF-7	breast:	n/a	n/a
37	BHLHE40	chr5:42908959-42909260	GM12878	blood:	n/a	n/a
38	CTCF	chr5:42908918-42909447	GM12878	blood:	n/a	n/a
39	ZNF143	chr5:42908583-42909333	H1-hESC	embryonic stem cell:	n/a	n/a
40	RAD21	chr5:42908931-42909379	ECC-1	luminal epithelium:	n/a	n/a
41	NRF1	chr5:42908557-42909430	SK-N-SH	brain:	n/a	chr5:42908869-42908883 chr5:42909110-42909121
42	SMC3	chr5:42908893-42909400	Hela-S3	cervix:	n/a	n/a
43	SMC3	chr5:42908586-42909478	SK-N-SH	brain:	n/a	n/a
44	CTCF	chr5:42909029-42909310	MCF-7	breast:	n/a	n/a
45	CTCF	chr5:42909008-42909316	ECC-1	luminal epithelium:	n/a	n/a
46	CTCF	chr5:42909030-42909302	Lung_OC	lung:	n/a	n/a
47	CTCF	chr5:42908918-42909378	H1-hESC	embryonic stem cell:	n/a	n/a
48	TCF12	chr5:42908696-42909459	A549	lung:	n/a	chr5:42909364-42909374 chr5:42909411-42909419
49	GTF2F1	chr5:42908729-42909328	K562	blood:	n/a	n/a
50	MAZ	chr5:42909026-42909386	GM12878	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:42908857..42910740-chr5:43065280..43068531,3	K562	blood:
2	chr5:42907363..42912501-chr5:43064737..43069149,8	MCF-7	breast:
3	chr5:42908654..42910895-chr5:43006900..43010047,5	MCF-7	breast:
4	chr5:42908870..42911135-chr5:43009033..43010803,2	K562	blood:
5	chr5:42908849..42909564-chr5:43064584..43065395,2	K562	blood:
6	chr5:42907010..42910562-chr5:43064999..43067630,3	MCF-7	breast:
7	chr5:42907581..42909848-chr5:43040254..43042169,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000251656	TF binding region
ENSG00000271788	Chromatin interaction
ENSG00000177738	Chromatin interaction
ENSG00000172262	Chromatin interaction
ENSG00000215068	Chromatin interaction

Extended variants
information (count: 117 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:105)

rs_ID	r²[population]
rs10472376	1.00[ASN][1000 genomes]
rs10941609	1.00[ASN][1000 genomes]
rs11744076	1.00[ASN][1000 genomes]
rs11746055	1.00[ASN][1000 genomes]
rs12516224	1.00[ASN][1000 genomes]
rs12521684	1.00[ASN][1000 genomes]
rs13361827	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs160331	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs160332	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16872962	1.00[ASN][1000 genomes]
rs16874465	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17300495	1.00[ASN][1000 genomes]
rs2444853	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2548363	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2548367	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2548368	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2603635	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2924818	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs309920	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs309928	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs309933	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs309937	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs309943	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs309944	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs309945	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs315247	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs315248	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs315259	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs315261	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs315265	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs315267	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs315268	0.92[EUR][1000 genomes]
rs315269	0.92[EUR][1000 genomes]
rs375476	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs377822	0.92[EUR][1000 genomes]
rs378886	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs387180	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs388377	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs399923	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs401102	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs401583	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs404899	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs408180	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs410225	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs424862	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs426335	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs427799	0.92[EUR][1000 genomes]
rs435255	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs435445	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55736023	1.00[ASN][1000 genomes]
rs55962848	1.00[ASN][1000 genomes]
rs55981030	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56027646	1.00[ASN][1000 genomes]
rs56035132	1.00[ASN][1000 genomes]
rs56092116	1.00[ASN][1000 genomes]
rs56289342	1.00[ASN][1000 genomes]
rs56307687	1.00[ASN][1000 genomes]
rs56346893	1.00[ASN][1000 genomes]
rs57643758	1.00[ASN][1000 genomes]
rs57792463	1.00[ASN][1000 genomes]
rs58933160	1.00[ASN][1000 genomes]
rs60087060	1.00[ASN][1000 genomes]
rs60244620	1.00[ASN][1000 genomes]
rs60303876	1.00[ASN][1000 genomes]
rs6887414	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72746737	1.00[ASN][1000 genomes]
rs72746739	1.00[ASN][1000 genomes]
rs72746746	1.00[ASN][1000 genomes]
rs72746753	1.00[ASN][1000 genomes]
rs72746762	1.00[ASN][1000 genomes]
rs72746766	1.00[ASN][1000 genomes]
rs72746768	1.00[ASN][1000 genomes]
rs72746770	1.00[ASN][1000 genomes]
rs72748850	1.00[ASN][1000 genomes]
rs72757078	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72757080	0.89[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs72759052	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759059	0.96[EUR][1000 genomes]
rs72759060	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759061	0.96[EUR][1000 genomes]
rs72759062	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759066	0.96[EUR][1000 genomes]
rs72759067	1.00[AFR][1000 genomes];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759071	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759072	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759073	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759075	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759084	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759085	0.80[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759086	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759087	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759093	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759095	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72759096	0.83[EUR][1000 genomes]
rs72759097	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72762696	1.00[ASN][1000 genomes]
rs72762697	1.00[ASN][1000 genomes]
rs72762698	1.00[ASN][1000 genomes]
rs72762701	1.00[ASN][1000 genomes]
rs72764507	1.00[ASN][1000 genomes]
rs72764510	1.00[ASN][1000 genomes]
rs72764515	1.00[ASN][1000 genomes]
rs72764524	1.00[ASN][1000 genomes]
rs73754528	1.00[ASN][1000 genomes]
rs7702086	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv993554	chr5:42720939-43251863	Bivalent/Poised TSS Strong transcription Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	298 gene(s)	inside rSNPs	diseases
2	nsv462126	chr5:42728831-43237188	Active TSS Enhancers Bivalent Enhancer Weak transcription Genic enhancers Flanking Active TSS Strong transcription 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	297 gene(s)	inside rSNPs	diseases
3	nsv597925	chr5:42728831-43237188	Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	297 gene(s)	inside rSNPs	diseases
4	nsv523033	chr5:42752037-42919685	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv1023741	chr5:42768215-43348145	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
6	nsv537737	chr5:42768215-43348145	Genic enhancers Enhancers Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	309 gene(s)	inside rSNPs	diseases
7	nsv534185	chr5:42804840-43067088	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	165 gene(s)	inside rSNPs	diseases
8	nsv1018276	chr5:42809131-42975245	Strong transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
9	nsv980936	chr5:42894375-42930741	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
10	nsv968909	chr5:42903982-42953465	Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
11	esv1806082	chr5:42906572-42967215	Transcr. at gene 5' and 3' Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
12	esv1813779	chr5:42906572-42992040	Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:42908400-42909200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
2	chr5:42908400-42909200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
3	chr5:42908400-42909200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
4	chr5:42908400-42909200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr5:42908400-42909200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr5:42908400-42909200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr5:42908400-42909200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr5:42908400-42909200	Flanking Active TSS	GM12878-XiMat	blood
9	chr5:42908400-42909200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr5:42908400-42909400	Flanking Active TSS	Liver	Liver
11	chr5:42908400-42909400	Active TSS	Brain Hippocampus Middle	brain
12	chr5:42908400-42909400	Flanking Active TSS	K562	blood
13	chr5:42908600-42909200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
14	chr5:42908600-42909200	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
15	chr5:42908600-42909200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr5:42908600-42909200	Bivalent/Poised TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr5:42908600-42909200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr5:42908600-42909200	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
19	chr5:42908600-42909200	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
20	chr5:42908600-42909200	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr5:42908600-42909200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
22	chr5:42908600-42909200	Flanking Active TSS	Primary B cells from peripheral blood	blood
23	chr5:42908600-42909200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
24	chr5:42908600-42909200	Active TSS	Primary T helper naive cells from peripheral blood	blood
25	chr5:42908600-42909200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
26	chr5:42908600-42909200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
27	chr5:42908600-42909200	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
28	chr5:42908600-42909200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
29	chr5:42908600-42909200	Flanking Active TSS	Adipose Nuclei	Adipose
30	chr5:42908600-42909200	Active TSS	Aorta	Aorta
31	chr5:42908600-42909200	Active TSS	Brain Inferior Temporal Lobe	brain
32	chr5:42908600-42909200	Bivalent/Poised TSS	Fetal Brain Male	brain
33	chr5:42908600-42909200	Flanking Bivalent TSS/Enh	Fetal Intestine Small	intestine
34	chr5:42908600-42909200	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
35	chr5:42908600-42909200	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
36	chr5:42908600-42909200	Flanking Active TSS	Placenta	Placenta
37	chr5:42908600-42909200	Active TSS	Lung	lung
38	chr5:42908600-42909200	Active TSS	Psoas Muscle	Psoas
39	chr5:42908600-42909200	Active TSS	Right Atrium	heart
40	chr5:42908600-42909200	Flanking Active TSS	HMEC	breast
41	chr5:42908600-42909200	Flanking Bivalent TSS/Enh	HUVEC	blood vessel
42	chr5:42908600-42909400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr5:42908600-42909400	Bivalent/Poised TSS	Fetal Brain Female	brain
44	chr5:42908600-42909400	Enhancers	Placenta Amnion	Placenta Amnion
45	chr5:42908800-42909200	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
46	chr5:42908800-42909200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr5:42908800-42909200	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
48	chr5:42908800-42909200	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr5:42908800-42909200	Active TSS	Breast Myoepithelial Primary Cells	Breast
50	chr5:42908800-42909200	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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