Variant report

Variant	rs455739
Chromosome Location	chr3:161089460-161089461
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:117)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:117 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF263	chr3:161089067-161091165	HEK293-T-REx	kidney:	n/a	chr3:161089773-161089782
2	CEBPB	chr3:161089060-161089748	MCF-7	breast:	n/a	n/a
3	POLR2A	chr3:161089028-161089651	MCF10A-Er-Src	breast:	n/a	n/a
4	ATF2	chr3:161089319-161089763	H1-hESC	embryonic stem cell:	n/a	n/a
5	GABPA	chr3:161089095-161091343	MCF-7	breast:	n/a	n/a
6	RAD21	chr3:161089368-161089911	H1-hESC	embryonic stem cell:	n/a	n/a
7	STAT3	chr3:161089344-161089513	MCF10A-Er-Src	breast:	n/a	chr3:161089493-161089505
8	TEAD4	chr3:161089292-161089787	H1-hESC	embryonic stem cell:	n/a	n/a
9	HDAC2	chr3:161089058-161091208	MCF-7	breast:	n/a	chr3:161089632-161089651
10	CTCF	chr3:161089460-161089610	A549	lung:	n/a	n/a
11	YY1	chr3:161089318-161089776	HCT-116	colon:	n/a	chr3:161089342-161089356 chr3:161089495-161089506
12	SP1	chr3:161089129-161089687	H1-hESC	embryonic stem cell:	n/a	chr3:161089495-161089507 chr3:161089495-161089506 chr3:161089342-161089354 chr3:161089344-161089353 chr3:161089343-161089353 chr3:161089342-161089354 chr3:161089343-161089352 chr3:161089497-161089506
13	GATA2	chr3:161089240-161091190	SH-SY5Y	brain:	n/a	chr3:161089781-161089790 chr3:161090986-161090996
14	EP300	chr3:161089035-161091712	MCF-7	breast:	n/a	chr3:161089801-161089817
15	YY1	chr3:161089345-161090140	H1-hESC	embryonic stem cell:	n/a	chr3:161089495-161089506
16	EP300	chr3:161089135-161089902	T-47D	breast:	n/a	chr3:161089801-161089817
17	EP300	chr3:161089126-161089830	T-47D	breast:	n/a	chr3:161089801-161089817
18	FOXA1	chr3:161089157-161089870	T-47D	breast:	n/a	n/a
19	TAF1	chr3:161088106-161091184	MCF-7	breast:	n/a	n/a
20	MYC	chr3:161089298-161089852	MCF-7	breast:	n/a	chr3:161089343-161089353
21	E2F6	chr3:161089363-161091367	H1-hESC	embryonic stem cell:	n/a	n/a
22	EGR1	chr3:161089035-161090168	HCT-116	colon:	n/a	chr3:161089796-161089809 chr3:161089422-161089433 chr3:161089422-161089432 chr3:161089416-161089438 chr3:161089422-161089433 chr3:161089422-161089432 chr3:161089420-161089434
23	CHD1	chr3:161089165-161089939	H1-hESC	embryonic stem cell:	n/a	chr3:161089497-161089507
24	REST	chr3:161089278-161091161	H1-neurons	neurons:	n/a	n/a
25	POLR2A	chr3:161089350-161090349	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD2	chr3:161089255-161089842	H1-hESC	embryonic stem cell:	n/a	chr3:161089497-161089507
27	FOSL2	chr3:161089080-161091306	MCF-7	breast:	n/a	chr3:161090986-161090995
28	EGR1	chr3:161089059-161091222	MCF-7	breast:	n/a	chr3:161089796-161089809 chr3:161089422-161089433 chr3:161089422-161089432 chr3:161089416-161089438 chr3:161089422-161089433 chr3:161089422-161089432 chr3:161089420-161089434 chr3:161090857-161090864
29	TEAD4	chr3:161089316-161089872	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr3:161089261-161091003	SK-N-SH	brain:	n/a	n/a
31	MAX	chr3:161089450-161091170	H1-hESC	embryonic stem cell:	n/a	n/a
32	RAD21	chr3:161089332-161089821	HepG2	liver:	n/a	n/a
33	POLR2A	chr3:161088975-161091192	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:161089440-161089590	BE2_C	brain:	n/a	n/a
35	GABPA	chr3:161089048-161091265	MCF-7	breast:	n/a	n/a
36	MYC	chr3:161089404-161090102	MCF-7	breast:	n/a	n/a
37	NANOG	chr3:161089386-161089678	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr3:161089140-161089875	HCT-116	colon:	n/a	n/a
39	ELF1	chr3:161089077-161091484	MCF-7	breast:	n/a	n/a
40	JUND	chr3:161089053-161091014	MCF-7	breast:	n/a	chr3:161090986-161090995
41	TCF12	chr3:161089245-161089902	ECC-1	luminal epithelium:	n/a	n/a
42	STAT3	chr3:161089225-161089595	MCF10A-Er-Src	breast:	n/a	chr3:161089493-161089505
43	REST	chr3:161088923-161090082	MCF-7	breast:	n/a	n/a
44	PML	chr3:161089034-161091298	MCF-7	breast:	n/a	n/a
45	POLR2A	chr3:161089383-161090003	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAX	chr3:161089346-161090161	H1-hESC	embryonic stem cell:	n/a	n/a
47	POLR2A	chr3:161089447-161089820	ECC-1	luminal epithelium:	n/a	n/a
48	RAD21	chr3:161089006-161091074	MCF-7	breast:	n/a	n/a
49	TCF12	chr3:161088987-161091243	MCF-7	breast:	n/a	n/a
50	GTF2F1	chr3:161089062-161089968	H1-hESC	embryonic stem cell:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:161089429-161089479	HCPEpiC	choroid plexus:	n/a
2	chr3:161089429-161089479	ECC-1	luminal epithelium:	n/a
3	chr3:161089429-161089479	SAEC	small airway:	n/a
4	chr3:161089429-161089479	A549	lung:	n/a
5	chr3:161089429-161089479	Hepatocyte	liver:	n/a
6	chr3:161089429-161089479	U87	brain:	n/a
7	chr3:161089429-161089479	HepG2	liver:	n/a
8	chr3:161089429-161089479	SK-N-SH_RA	brain:	n/a
9	chr3:161089429-161089479	BJ	skin:	n/a
10	chr3:161089429-161089479	CMK	blood:	n/a
11	chr3:161089429-161089479	SKMC	muscle:	n/a
12	chr3:161089429-161089479	AoSMC	blood vessel:	n/a
13	chr3:161089429-161089479	HUVEC	blood vessel:	n/a
14	chr3:161089429-161089479	RPTEC	kidney:	n/a
15	chr3:161089429-161089479	HEK293	kidney:	embryo
16	chr3:161089429-161089479	GM12892	blood:	n/a
17	chr3:161089429-161089479	NT2-D1	testis:	n/a
18	chr3:161089429-161089479	GM06990	blood:	n/a
19	chr3:161089429-161089479	HEEpiC	esophagus:	n/a
20	chr3:161089429-161089479	HCF	heart:	n/a
21	chr3:161089429-161089479	GM12891	blood:	n/a
22	chr3:161089429-161089479	NHBE	bronchial:	n/a
23	chr3:161089429-161089479	AG04450	lung:	fetal
24	chr3:161089429-161089479	H1-hESC	embryonic stem cell:	embryo
25	chr3:161089429-161089479	PFSK-1	brain:	n/a
26	chr3:161089429-161089479	NHDF-neo	bronchial:	n/a
27	chr3:161089429-161089479	HIPEpiC	eye:	n/a
28	chr3:161089429-161089479	GM19239	blood:	n/a
29	chr3:161089429-161089479	HL-60	blood:	n/a
30	chr3:161089429-161089479	Caco-2	colon:	n/a
31	chr3:161089429-161089479	HCT-116	colon:	n/a
32	chr3:161089429-161089479	K562	blood:	n/a
33	chr3:161089429-161089479	MCF10A-Er-Src	breast:	n/a
34	chr3:161089429-161089479	HRPEpiC	eye:	n/a
35	chr3:161089429-161089479	BE2_C	brain:	n/a
36	chr3:161089429-161089479	HRCEpiC	kidney:	n/a
37	chr3:161089429-161089479	NB4	blood:	n/a
38	chr3:161089429-161089479	AG04449	skin:	fetal
39	chr3:161089429-161089479	SK-N-MC	brain:	n/a
40	chr3:161089429-161089479	ProgFib	skin:	n/a
41	chr3:161089429-161089479	HCM	heart:	n/a
42	chr3:161089429-161089479	IMR90	lung:	fetal
43	chr3:161089429-161089479	SK-N-SH	brain:	n/a
44	chr3:161089429-161089479	HNPCEpiC	eye:	n/a
45	chr3:161089429-161089479	GM12878	blood:	n/a
46	chr3:161089429-161089479	HPAEpiC	pulmonary alveolar:	n/a
47	chr3:161089429-161089479	HMEC	breast:	n/a
48	chr3:161089429-161089479	MCF-7	breast:	n/a
49	chr3:161089429-161089479	Hela-S3	cervix:	n/a
50	chr3:161089429-161089479	LNCaP	prostate:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:160282107..160285570-chr3:161087865..161089951,3	MCF-7	breast:
2	chr3:161038392..161046344-chr3:161085640..161093564,25	MCF-7	breast:
3	chr3:160934982..160947568-chr3:161079696..161093037,40	MCF-7	breast:
4	chr20:31169325..31171437-chr3:161088010..161089511,2	MCF-7	breast:
5	chr22:31475291..31477772-chr3:161087457..161089639,2	MCF-7	breast:
6	chr13:37572263..37575251-chr3:161088174..161090196,2	MCF-7	breast:
7	chr20:45982415..45984680-chr3:161089076..161091449,2	MCF-7	breast:
8	chr3:136470318..136472005-chr3:161088059..161090755,2	MCF-7	breast:
9	chr3:160936365..160960187-chr3:161078472..161094658,51	MCF-7	breast:
10	chr17:58040687..58043660-chr3:161087957..161089475,2	MCF-7	breast:
11	chr2:97535160..97536953-chr3:161088031..161090726,2	MCF-7	breast:
12	chr3:161089431..161091438-chr6:26196434..26199354,2	MCF-7	breast:
13	chr3:161088166..161091113-chr7:44082932..44085823,2	MCF-7	breast:
14	chr12:48212981..48215317-chr3:161089373..161090906,2	MCF-7	breast:
15	chr17:57181517..57184200-chr3:161086879..161089854,2	MCF-7	breast:
16	chr3:161089389..161090264-chr3:161126588..161127432,3	MCF-7	breast:
17	chr3:160813033..160824577-chr3:161083489..161092050,35	MCF-7	breast:
18	chr3:161087384..161090083-chr9:131900097..131902606,2	MCF-7	breast:
19	chr3:160472518..160475131-chr3:161089184..161091851,3	MCF-7	breast:
20	chr22:30683032..30685513-chr3:161089094..161092006,2	MCF-7	breast:
21	chr14:73955822..73958124-chr3:161089151..161090979,2	MCF-7	breast:
22	chr20:49346270..49349571-chr3:161087854..161090885,3	MCF-7	breast:
23	chr20:56282039..56284863-chr3:161089358..161091881,2	MCF-7	breast:
24	chr3:161088340..161091318-chr9:131938931..131941651,2	MCF-7	breast:
25	chr1:149858017..149860169-chr3:161088036..161090033,2	MCF-7	breast:
26	chr3:160587600..160589495-chr3:161088974..161091016,2	MCF-7	breast:
27	chr3:161087820..161090854-chr7:26238154..26241381,3	MCF-7	breast:
28	chr12:12713891..12716367-chr3:161087265..161090021,2	MCF-7	breast:
29	chr3:161088194..161090248-chr9:137216086..137218582,2	MCF-7	breast:

No data

Variant related genes	Relation type
SPTSSB	TF binding region
SPTSSB	CpG island
ENSG00000260572	Chromatin interaction
ENSG00000122565	Chromatin interaction
ENSG00000168758	Chromatin interaction
ENSG00000061273	Chromatin interaction
ENSG00000136279	Chromatin interaction
ENSG00000118007	Chromatin interaction
ENSG00000183963	Chromatin interaction
ENSG00000197409	Chromatin interaction
ENSG00000111266	Chromatin interaction
ENSG00000108395	Chromatin interaction
ENSG00000224738	Chromatin interaction
ENSG00000204055	Chromatin interaction
ENSG00000228156	Chromatin interaction
ENSG00000120697	Chromatin interaction
ENSG00000169251	Chromatin interaction
ENSG00000261758	Chromatin interaction
ENSG00000186432	Chromatin interaction
ENSG00000184270	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000163590	Chromatin interaction
ENSG00000124225	Chromatin interaction
ENSG00000271052	Chromatin interaction
ENSG00000186350	Chromatin interaction
ENSG00000119383	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000267302	Chromatin interaction
ENSG00000239282	Chromatin interaction
ENSG00000240138	Chromatin interaction
ENSG00000169255	Chromatin interaction
ENSG00000184260	Chromatin interaction
ENSG00000184678	Chromatin interaction
ENSG00000178096	Chromatin interaction
ENSG00000189050	Chromatin interaction
ENSG00000170468	Chromatin interaction
ENSG00000188483	Chromatin interaction
ENSG00000255242	Chromatin interaction
ENSG00000120699	Chromatin interaction
ENSG00000229320	Chromatin interaction
ENSG00000122566	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs12488318	0.85[ASN][1000 genomes]
rs12494261	0.86[ASN][1000 genomes]
rs1450519	0.86[ASN][1000 genomes]
rs1471440	0.90[ASN][1000 genomes]
rs1478567	0.86[ASN][1000 genomes]
rs163138	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs336544	0.91[ASN][1000 genomes]
rs336545	0.91[ASN][1000 genomes]
rs336546	0.91[ASN][1000 genomes]
rs336564	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs336565	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs336566	0.98[ASN][1000 genomes]
rs336571	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs336573	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs336574	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs336576	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs336581	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs336584	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs336587	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs336588	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs336592	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs419703	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs458197	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs459067	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs461616	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs462081	1.00[ASN][1000 genomes]
rs57201455	0.90[ASN][1000 genomes]
rs73162530	0.90[ASN][1000 genomes]
rs9290075	0.85[ASN][1000 genomes]
rs978933	0.90[ASN][1000 genomes]
rs9811833	0.91[ASN][1000 genomes]
rs9812083	0.86[ASN][1000 genomes]
rs9827833	0.83[ASN][1000 genomes]
rs9828189	0.86[ASN][1000 genomes]
rs9828231	0.81[ASN][1000 genomes]
rs9839404	0.86[ASN][1000 genomes]
rs9859045	0.86[ASN][1000 genomes]
rs9876553	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv931072	chr3:160669567-161159779	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
2	nsv533237	chr3:161019834-161804660	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	91 gene(s)	inside rSNPs	diseases
3	nsv829772	chr3:161047817-161202554	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	88 gene(s)	inside rSNPs	diseases
4	nsv877710	chr3:161087857-161245414	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	84 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:161088000-161091400	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr3:161088400-161089800	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr3:161088400-161091000	Active TSS	H9 Cell Line	embryonic stem cell
4	chr3:161088600-161090600	Active TSS	H1 Cell Line	embryonic stem cell
5	chr3:161088600-161090600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
6	chr3:161088600-161090800	Active TSS	Stomach Mucosa	stomach
7	chr3:161089000-161089600	Flanking Active TSS	Fetal Brain Female	brain
8	chr3:161089000-161090200	Active TSS	HUES48 Cell Line	embryonic stem cell
9	chr3:161089000-161090400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
10	chr3:161089000-161090600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
11	chr3:161089000-161090600	Active TSS	Brain Anterior Caudate	brain
12	chr3:161089000-161090600	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr3:161089000-161090600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
14	chr3:161089000-161090800	Active TSS	Brain Germinal Matrix	brain
15	chr3:161089000-161091000	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:161089000-161091000	Active TSS	Brain Cingulate Gyrus	brain
17	chr3:161089200-161089600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr3:161089200-161089600	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr3:161089200-161089600	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr3:161089200-161089600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
21	chr3:161089200-161089600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
22	chr3:161089200-161089600	Flanking Bivalent TSS/Enh	Muscle Satellite Cultured Cells	--
23	chr3:161089200-161089600	Flanking Active TSS	Brain Substantia Nigra	brain
24	chr3:161089200-161089600	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
25	chr3:161089200-161089600	Flanking Active TSS	Fetal Brain Male	brain
26	chr3:161089200-161089600	Bivalent Enhancer	Fetal Heart	heart
27	chr3:161089200-161089600	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
28	chr3:161089200-161089600	Active TSS	Placenta Amnion	Placenta Amnion
29	chr3:161089200-161089600	Bivalent Enhancer	HSMM	muscle
30	chr3:161089200-161089800	Bivalent Enhancer	Primary B cells from cord blood	blood
31	chr3:161089200-161089800	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
32	chr3:161089200-161089800	Flanking Bivalent TSS/Enh	Primary T killer naive cells fromperipheralblood	blood
33	chr3:161089200-161089800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr3:161089200-161089800	Flanking Active TSS	Brain Hippocampus Middle	brain
35	chr3:161089200-161089800	Flanking Active TSS	Right Atrium	heart
36	chr3:161089200-161090000	Bivalent Enhancer	Primary B cells from peripheral blood	blood
37	chr3:161089200-161090000	Bivalent/Poised TSS	Psoas Muscle	Psoas
38	chr3:161089200-161090000	Bivalent/Poised TSS	HepG2	liver
39	chr3:161089200-161090200	Active TSS	iPS-18 Cell Line	embryonic stem cell
40	chr3:161089200-161090200	Bivalent/Poised TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr3:161089200-161090200	Flanking Bivalent TSS/Enh	Primary T helper cells PMA-I stimulated	--
42	chr3:161089200-161090200	Flanking Bivalent TSS/Enh	Primary T helper 17 cells PMA-I stimulated	--
43	chr3:161089200-161090200	Flanking Bivalent TSS/Enh	Primary T regulatory cells fromperipheralblood	blood
44	chr3:161089200-161090200	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
45	chr3:161089200-161090400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr3:161089200-161090400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr3:161089200-161090400	Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr3:161089200-161090600	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:161089200-161090600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
50	chr3:161089200-161090600	Bivalent/Poised TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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