Variant report

Variant	rs12495866
Chromosome Location	chr3:19988182-19988183
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	POLR2A	chr3:19987362-19989595	K562	blood:	n/a	n/a
2	HCFC1	chr3:19987605-19989689	K562	blood:	n/a	n/a
3	RUNX3	chr3:19987795-19989519	GM12878	blood:	n/a	n/a
4	POLR2A	chr3:19987558-19989602	GM18951	blood:	n/a	n/a
5	POLR2A	chr3:19986887-19989909	GM12891	blood:	n/a	n/a
6	STAT1	chr3:19987955-19989668	GM12878	blood:	n/a	chr3:19988530-19988542 chr3:19989252-19989264 chr3:19989188-19989197 chr3:19988321-19988329 chr3:19989110-19989122
7	SIN3AK20	chr3:19987338-19989938	MCF-7	breast:	n/a	n/a
8	YY1	chr3:19987952-19988608	K562	blood:	n/a	chr3:19987999-19988008 chr3:19988151-19988159
9	EGR1	chr3:19988040-19988966	K562	blood:	n/a	chr3:19988337-19988347 chr3:19988633-19988642 chr3:19988244-19988254 chr3:19988611-19988621
10	EP300	chr3:19988051-19989533	GM12878	blood:	n/a	chr3:19989189-19989198 chr3:19988330-19988346 chr3:19988621-19988637
11	HEY1	chr3:19987858-19989594	K562	blood:	n/a	n/a
12	CREB1	chr3:19988089-19989745	HepG2	liver:	n/a	n/a
13	BCL3	chr3:19987604-19988689	A549	lung:	n/a	chr3:19988323-19988332 chr3:19988611-19988624 chr3:19988633-19988642
14	CEBPD	chr3:19988180-19988727	HepG2	liver:	n/a	n/a
15	POLR2A	chr3:19988117-19989553	MCF-7	breast:	n/a	n/a
16	MAX	chr3:19987921-19989653	HepG2	liver:	n/a	chr3:19988609-19988619 chr3:19989189-19989198
17	JUN	chr3:19987484-19988866	K562	blood:	n/a	n/a
18	SMARCC1	chr3:19986964-19989766	Hela-S3	cervix:	n/a	chr3:19989188-19989197 chr3:19989189-19989198
19	NFIC	chr3:19988124-19988671	HepG2	liver:	n/a	n/a
20	SIN3AK20	chr3:19988033-19989755	K562	blood:	n/a	n/a
21	POLR2A	chr3:19987474-19989718	GM12878	blood:	n/a	n/a
22	USF2	chr3:19988148-19989015	H1-hESC	embryonic stem cell:	n/a	chr3:19988614-19988630 chr3:19988464-19988475
23	MAX	chr3:19988142-19989678	MCF-7	breast:	n/a	chr3:19988609-19988619 chr3:19989189-19989198
24	TAF1	chr3:19987982-19988474	Hela-S3	cervix:	n/a	n/a
25	FOXM1	chr3:19987637-19989053	GM12878	blood:	n/a	n/a
26	POLR2A	chr3:19987476-19989652	U87	brain:	n/a	n/a
27	POLR2A	chr3:19987594-19989784	GM18505	blood:	n/a	n/a
28	HMGN3	chr3:19987829-19989561	K562	blood:	n/a	chr3:19989190-19989199
29	YY1	chr3:19988002-19989624	NT2-D1	testis:	n/a	chr3:19988611-19988625 chr3:19989269-19989277 chr3:19988611-19988620 chr3:19988151-19988159 chr3:19989258-19989280
30	RCOR1	chr3:19987828-19988777	Hela-S3	cervix:	n/a	n/a
31	YY1	chr3:19987941-19988686	GM12892	blood:	n/a	chr3:19988611-19988625 chr3:19988611-19988620 chr3:19987999-19988008 chr3:19988151-19988159
32	USF1	chr3:19988065-19988850	A549	lung:	n/a	chr3:19988614-19988630 chr3:19988464-19988475
33	TAF1	chr3:19987928-19988376	GM12878	blood:	n/a	n/a
34	BCLAF1	chr3:19988104-19988997	K562	blood:	n/a	chr3:19988323-19988332 chr3:19988611-19988624 chr3:19988633-19988642
35	GABPA	chr3:19988130-19989410	SK-N-SH	brain:	n/a	chr3:19988538-19988545
36	BRCA1	chr3:19988073-19989122	GM12878	blood:	n/a	n/a
37	POLR2A	chr3:19987565-19989776	MCF-7	breast:	n/a	n/a
38	POLR2A	chr3:19987429-19989814	H1-hESC	embryonic stem cell:	n/a	n/a
39	BHLHE40	chr3:19987806-19989437	GM12878	blood:	n/a	chr3:19988614-19988630
40	REST	chr3:19987805-19989021	A549	lung:	n/a	n/a
41	TBP	chr3:19986938-19989974	K562	blood:	n/a	n/a
42	MAX	chr3:19987976-19989165	H1-hESC	embryonic stem cell:	n/a	chr3:19988609-19988619
43	MEF2A	chr3:19987741-19988852	GM12878	blood:	n/a	n/a
44	YY1	chr3:19987910-19989745	K562	blood:	n/a	chr3:19988611-19988625 chr3:19989269-19989277 chr3:19988611-19988620 chr3:19987999-19988008 chr3:19988151-19988159 chr3:19989258-19989280
45	TAF1	chr3:19987973-19989612	H1-neurons	neurons:	n/a	n/a
46	CHD2	chr3:19987637-19989399	H1-hESC	embryonic stem cell:	n/a	chr3:19989363-19989373
47	WRNIP1	chr3:19987590-19989775	GM12878	blood:	n/a	n/a
48	POLR2A	chr3:19987007-19989845	K562	blood:	n/a	n/a
49	E2F4	chr3:19987975-19989588	K562	blood:	n/a	chr3:19988690-19988700 chr3:19987999-19988008 chr3:19988611-19988620 chr3:19987996-19988008 chr3:19988615-19988625
50	POLR2A	chr3:19986884-19989655	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:19988132-19988182	GM12892	blood:	n/a
2	chr3:19988132-19988182	ovcar-3	ovarian:	n/a
3	chr3:19988132-19988182	T-47D	breast:	n/a
4	chr3:19988132-19988182	K562	blood:	n/a
5	chr3:19988132-19988182	AG04449	skin:	fetal
6	chr3:19988132-19988182	PANC-1	pancreas:	n/a
7	chr3:19988132-19988182	HL-60	blood:	n/a
8	chr3:19988132-19988182	MCF10A-Er-Src	breast:	n/a
9	chr3:19988132-19988182	SAEC	small airway:	n/a
10	chr3:19988132-19988182	HEEpiC	esophagus:	n/a
11	chr3:19988132-19988182	H1-hESC	embryonic stem cell:	embryo
12	chr3:19988132-19988182	AG09319	gingival:	n/a
13	chr3:19988132-19988182	U87	brain:	n/a
14	chr3:19988132-19988182	CMK	blood:	n/a
15	chr3:19988132-19988182	GM12891	blood:	n/a
16	chr3:19988132-19988182	GM12878	blood:	n/a
17	chr3:19988132-19988182	GM19239	blood:	n/a
18	chr3:19988132-19988182	ECC-1	luminal epithelium:	n/a
19	chr3:19988132-19988182	HCF	heart:	n/a
20	chr3:19988132-19988182	BJ	skin:	n/a
21	chr3:19988132-19988182	A549	lung:	n/a
22	chr3:19988132-19988182	SK-N-SH_RA	brain:	n/a
23	chr3:19988132-19988182	IMR90	lung:	fetal
24	chr3:19988132-19988182	Hela-S3	cervix:	n/a
25	chr3:19988132-19988182	HIPEpiC	eye:	n/a
26	chr3:19988132-19988182	NB4	blood:	n/a
27	chr3:19988132-19988182	AG04450	lung:	fetal
28	chr3:19988132-19988182	AG09309	skin:	n/a
29	chr3:19988132-19988182	HRE	kidney:	n/a
30	chr3:19988132-19988182	NH-A	brain:	n/a
31	chr3:19988132-19988182	HMEC	breast:	n/a
32	chr3:19988132-19988182	Jurkat	blood:	n/a
33	chr3:19988132-19988182	HNPCEpiC	eye:	n/a
34	chr3:19988132-19988182	Caco-2	colon:	n/a
35	chr3:19988132-19988182	HepG2	liver:	n/a
36	chr3:19988132-19988182	HCM	heart:	n/a
37	chr3:19988132-19988182	PrEC	prostate:	n/a
38	chr3:19988132-19988182	HEK293	kidney:	embryo
39	chr3:19988132-19988182	BE2_C	brain:	n/a
40	chr3:19988132-19988182	SK-N-MC	brain:	n/a
41	chr3:19988132-19988182	HPAEpiC	pulmonary alveolar:	n/a
42	chr3:19988132-19988182	SKMC	muscle:	n/a
43	chr3:19988132-19988182	LNCaP	prostate:	n/a
44	chr3:19988132-19988182	SK-N-SH	brain:	n/a
45	chr3:19988132-19988182	HUVEC	blood vessel:	n/a
46	chr3:19988132-19988182	AoSMC	blood vessel:	n/a
47	chr3:19988132-19988182	MCF-7	breast:	n/a
48	chr3:19988132-19988182	RPTEC	kidney:	n/a
49	chr3:19988132-19988182	NT2-D1	testis:	n/a
50	chr3:19988132-19988182	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:19986921..19992254-chr3:20078952..20084327,16	K562	blood:
2	chr3:19987782..19990680-chr3:20013275..20017779,4	K562	blood:
3	chr17:8076548..8077059-chr3:19987723..19988396,2	Hela-S3	cervix:
4	chr3:19987383..19992426-chr3:20011245..20019650,13	MCF-7	breast:
5	chr3:19987439..19992261-chr3:20226257..20229350,4	K562	blood:
6	chr3:19987513..19990087-chr3:20080861..20083140,3	MCF-7	breast:
7	chr3:19985145..19990136-chr3:20225418..20228312,6	K562	blood:
8	chr3:19975611..19979082-chr3:19987774..19990681,3	MCF-7	breast:
9	chr1:155107729..155108614-chr3:19988180..19988972,2	Hela-S3	cervix:
10	chr3:19188168..19190474-chr3:19988134..19989911,2	MCF-7	breast:
11	chr3:19986985..19992254-chr3:20079680..20083856,14	K562	blood:

Variant related genes	Relation type
HSPA8P18	TF binding region
RAB5A	TF binding region
HSPA8P18	CpG island
RAB5A	CpG island
ENSG00000169241	Chromatin interaction
ENSG00000129810	Chromatin interaction
ENSG00000200463	Chromatin interaction
ENSG00000144566	Chromatin interaction
ENSG00000183960	Chromatin interaction
ENSG00000114166	Chromatin interaction
ENSG00000163576	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10510497	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12374092	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12486167	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12486526	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12488378	1.00[ASN][1000 genomes]
rs12490848	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12497549	1.00[ASN][1000 genomes]
rs17006416	0.90[AFR][1000 genomes]
rs17006418	0.90[AFR][1000 genomes]
rs17006433	0.90[AFR][1000 genomes]
rs17006435	0.90[AFR][1000 genomes]
rs17006443	0.88[AFR][1000 genomes]
rs17181337	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17796230	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2365374	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28597881	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2866630	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4241539	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4398451	1.00[ASN][1000 genomes]
rs45542931	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4618239	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858116	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858632	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858662	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858664	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4858674	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55797296	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55892327	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56029370	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56994247	0.90[AFR][1000 genomes]
rs57181336	0.90[AFR][1000 genomes]
rs57382802	0.90[AFR][1000 genomes]
rs59361244	0.90[AFR][1000 genomes]
rs61255313	0.90[AFR][1000 genomes]
rs62241279	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62241280	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62241285	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62241286	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62241289	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62241295	0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62241316	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62241322	0.95[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62241326	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62241330	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62241333	1.00[ASN][1000 genomes]
rs62241334	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62241337	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62243065	1.00[ASN][1000 genomes]
rs62243074	1.00[ASN][1000 genomes]
rs62243075	1.00[ASN][1000 genomes]
rs62243076	1.00[ASN][1000 genomes]
rs73032477	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73034166	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	nsv1010123	chr3:18990307-19989504	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv433358	chr3:19547184-19996508	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	esv1828161	chr3:19547184-20062060	Flanking Active TSS Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	esv1825914	chr3:19549859-20137270	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
5	esv1833006	chr3:19562271-20389045	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
6	esv1826570	chr3:19579860-20077414	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	esv1833139	chr3:19579860-20121349	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	esv1826254	chr3:19592688-20042834	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
9	nsv1010613	chr3:19942032-20461486	Weak transcription Active TSS Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
10	esv1826030	chr3:19972766-20170581	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers 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	15 gene(s)	inside rSNPs	diseases
11	esv1825988	chr3:19976375-20102773	Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Active TSS Genic enhancers 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	15 gene(s)	inside rSNPs	diseases
12	esv1826830	chr3:19982972-20632072	Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 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	chr3:19986800-19990200	Active TSS	Duodenum Mucosa	Duodenum
2	chr3:19987000-19989600	Active TSS	Liver	Liver
3	chr3:19987200-19989000	Active TSS	HepG2	liver
4	chr3:19987200-19989800	Active TSS	Pancreas	Pancrea
5	chr3:19987200-19990400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:19987200-19990400	Active TSS	Placenta	Placenta
7	chr3:19987200-19990600	Active TSS	K562	blood
8	chr3:19987200-19991800	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr3:19987400-19988200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
10	chr3:19987400-19988200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
11	chr3:19987400-19988200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr3:19987400-19988200	Flanking Active TSS	Dnd41	blood
13	chr3:19987400-19988800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr3:19987400-19989000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr3:19987400-19989200	Active TSS	Skeletal Muscle Female	skeletal muscle
16	chr3:19987400-19989400	Active TSS	Brain Anterior Caudate	brain
17	chr3:19987400-19989400	Active TSS	Brain Inferior Temporal Lobe	brain
18	chr3:19987400-19989400	Active TSS	Rectal Smooth Muscle	rectum
19	chr3:19987400-19989800	Active TSS	Sigmoid Colon	Sigmoid Colon
20	chr3:19987400-19990000	Active TSS	Brain Germinal Matrix	brain
21	chr3:19987400-19990000	Active TSS	Duodenum Smooth Muscle	Duodenum
22	chr3:19987400-19990000	Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr3:19987400-19990000	Active TSS	A549	lung
24	chr3:19987400-19990200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr3:19987400-19990200	Active TSS	HSMM	muscle
26	chr3:19987400-19990400	Active TSS	NHDF-Ad	bronchial
27	chr3:19987400-19990800	Active TSS	Right Atrium	heart
28	chr3:19987400-19990800	Active TSS	HSMMtube	muscle
29	chr3:19987400-19991400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr3:19987600-19988200	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr3:19987600-19988200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr3:19987600-19988200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:19987600-19988200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
34	chr3:19987600-19988200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
35	chr3:19987600-19988200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
36	chr3:19987600-19988200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
37	chr3:19987600-19988200	Flanking Active TSS	Primary B cells from cord blood	blood
38	chr3:19987600-19988200	Flanking Active TSS	Primary B cells from peripheral blood	blood
39	chr3:19987600-19988200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
40	chr3:19987600-19988200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
41	chr3:19987600-19988200	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
42	chr3:19987600-19988200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:19987600-19988200	Flanking Active TSS	Adipose Nuclei	Adipose
44	chr3:19987600-19988200	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
45	chr3:19987600-19988200	Flanking Active TSS	Fetal Muscle Leg	muscle
46	chr3:19987600-19988200	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
47	chr3:19987600-19988200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
48	chr3:19987600-19988200	Flanking Active TSS	NH-A	brain
49	chr3:19987600-19988200	Flanking Active TSS	Osteobl	bone
50	chr3:19987600-19988400	Flanking Active TSS	Primary T cells fromperipheralblood	blood

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