Variant report

Variant	rs9289566
Chromosome Location	chr3:138554297-138554298
allele	C/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	TCF7L2	chr3:138553254-138554404	PANC-1	pancreas:	n/a	n/a
2	TAF1	chr3:138553521-138554347	ECC-1	luminal epithelium:	n/a	n/a
3	TCF12	chr3:138553724-138554314	A549	lung:	n/a	chr3:138554242-138554249 chr3:138553799-138553809
4	POLR2A	chr3:138553440-138554683	HepG2	liver:	n/a	n/a
5	JUND	chr3:138552223-138554440	K562	blood:	n/a	chr3:138552948-138552957 chr3:138553808-138553817
6	POLR2A	chr3:138552175-138554448	K562	blood:	n/a	n/a
7	TAF1	chr3:138553079-138554356	H1-hESC	embryonic stem cell:	n/a	n/a
8	EP300	chr3:138552943-138554448	ECC-1	luminal epithelium:	n/a	chr3:138553618-138553627 chr3:138554197-138554210 chr3:138553551-138553560 chr3:138553744-138553753 chr3:138553473-138553482 chr3:138553549-138553565 chr3:138553514-138553530
9	REST	chr3:138552889-138554705	H1-neurons	neurons:	n/a	chr3:138554533-138554542 chr3:138553694-138553707 chr3:138553308-138553317
10	RCOR1	chr3:138554108-138554534	K562	blood:	n/a	n/a
11	HA-E2F1	chr3:138552844-138554368	MCF-7	breast:	n/a	chr3:138553487-138553497 chr3:138553802-138553812 chr3:138553740-138553749 chr3:138553551-138553561 chr3:138553701-138553710 chr3:138553473-138553483 chr3:138553470-138553480
12	USF2	chr3:138553982-138554436	K562	blood:	n/a	n/a
13	POLR2A	chr3:138553050-138554316	H1-neurons	neurons:	n/a	n/a
14	POLR2A	chr3:138552346-138554538	PBDE	blood:	n/a	n/a
15	POLR2A	chr3:138552492-138554386	GM12878	blood:	n/a	n/a
16	POLR2A	chr3:138553334-138554428	U87	brain:	n/a	n/a
17	MAZ	chr3:138552401-138554328	K562	blood:	n/a	n/a
18	GTF2F1	chr3:138553817-138554401	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr3:138550642-138554801	K562	blood:	n/a	n/a
20	HEY1	chr3:138552972-138554354	K562	blood:	n/a	chr3:138553465-138553480 chr3:138553821-138553836 chr3:138553549-138553564 chr3:138553280-138553295 chr3:138553703-138553718
21	MAX	chr3:138553716-138554318	SK-N-SH	brain:	n/a	n/a
22	POLR2A	chr3:138553054-138554391	GM15510	blood:	n/a	n/a
23	EP300	chr3:138553314-138554366	SK-N-SH	brain:	n/a	chr3:138553618-138553627 chr3:138554197-138554210 chr3:138553551-138553560 chr3:138553744-138553753 chr3:138553473-138553482 chr3:138553549-138553565 chr3:138553514-138553530
24	POLR2A	chr3:138552834-138554443	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr3:138552554-138554416	K562	blood:	n/a	n/a
26	MAX	chr3:138552730-138554459	HepG2	liver:	n/a	n/a
27	POLR2A	chr3:138552339-138554314	K562	blood:	n/a	n/a
28	TBP	chr3:138552407-138554341	K562	blood:	n/a	n/a
29	POLR2A	chr3:138551067-138554365	K562	blood:	n/a	n/a
30	POLR2A	chr3:138553035-138554712	GM18505	blood:	n/a	n/a
31	MYBL2	chr3:138553687-138554624	HepG2	liver:	n/a	n/a
32	POLR2A	chr3:138552893-138554676	H1-hESC	embryonic stem cell:	n/a	n/a
33	MYC	chr3:138552225-138554485	K562	blood:	n/a	n/a
34	POLR2A	chr3:138553303-138554448	SK-N-MC	brain:	n/a	n/a
35	POLR2A	chr3:138552611-138554605	GM12891	blood:	n/a	n/a
36	POLR2A	chr3:138553213-138554566	Hela-S3	cervix:	n/a	n/a
37	POLR2A	chr3:138552865-138554453	HepG2	liver:	n/a	n/a
38	REST	chr3:138553434-138554384	H1-neurons	neurons:	n/a	chr3:138553694-138553707
39	CUX1	chr3:138554070-138554335	K562	blood:	n/a	n/a
40	HEY1	chr3:138553064-138554577	HepG2	liver:	n/a	chr3:138553465-138553480 chr3:138553821-138553836 chr3:138553549-138553564 chr3:138553280-138553295 chr3:138553703-138553718
41	POLR2A	chr3:138553211-138554525	HepG2	liver:	n/a	n/a
42	MAX	chr3:138552880-138554298	A549	lung:	n/a	n/a
43	MXI1	chr3:138552369-138554357	HepG2	liver:	n/a	n/a
44	POLR2A	chr3:138553027-138554662	K562	blood:	n/a	n/a
45	MAX	chr3:138552391-138554393	Hela-S3	cervix:	n/a	n/a
46	NFIC	chr3:138553837-138554301	HepG2	liver:	n/a	n/a
47	MYBL2	chr3:138553011-138554362	HepG2	liver:	n/a	n/a
48	POLR2A	chr3:138553045-138554303	GM18951	blood:	n/a	n/a
49	MYC	chr3:138552234-138554378	K562	blood:	n/a	n/a
50	POLR2A	chr3:138553214-138554318	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:138553797..138555960-chr3:138598138..138600170,2	K562	blood:
2	chr3:138541276..138545209-chr3:138550830..138554565,5	MCF-7	breast:
3	chr2:88315513..88316151-chr3:138553830..138554380,2	Hela-S3	cervix:
4	chr3:138552568..138555141-chr3:138666105..138668600,2	K562	blood:
5	chr3:138552259..138555153-chr3:138660631..138662853,2	K562	blood:
6	chr3:138552263..138555163-chr3:138665790..138667540,3	K562	blood:
7	chr3:138326713..138328588-chr3:138552751..138555574,2	MCF-7	breast:
8	chr3:138433313..138434820-chr3:138553042..138555465,2	MCF-7	breast:

Variant related genes	Relation type
PIK3CB	TF binding region
ENSG00000222724	Chromatin interaction
ENSG00000183770	Chromatin interaction
ENSG00000206262	Chromatin interaction
ENSG00000241429	Chromatin interaction
ENSG00000158234	Chromatin interaction
ENSG00000244578	Chromatin interaction
ENSG00000051382	Chromatin interaction

Extended variants
information (count: 108 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:97)

rs_ID	r²[population]
rs1068685	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs10804659	0.92[EUR][1000 genomes]
rs10935288	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11705762	0.81[EUR][1000 genomes]
rs11706016	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs11708762	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11711360	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11713049	0.80[EUR][1000 genomes]
rs11720178	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes]
rs11924479	0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11924814	0.80[EUR][1000 genomes]
rs12497815	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12631035	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12633714	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs12635713	0.81[EUR][1000 genomes]
rs13061496	0.96[CEU][hapmap];0.87[EUR][1000 genomes]
rs13072146	0.84[EUR][1000 genomes]
rs13077455	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13082808	0.81[EUR][1000 genomes]
rs13100110	0.81[EUR][1000 genomes]
rs1400266	0.80[EUR][1000 genomes]
rs1663554	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs1673597	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs17484361	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs191714	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs191775	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs2607796	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs28408150	0.81[EUR][1000 genomes]
rs2881900	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs35214574	0.81[EUR][1000 genomes]
rs361057	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs361059	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs361060	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs361061	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs361062	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs361063	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs361066	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs361067	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs361071	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs361072	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs361080	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs361082	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs361087	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs361088	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs361096	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs371762	0.81[EUR][1000 genomes]
rs385254	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs413147	0.96[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs4305444	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs4405948	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4894358	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4894359	1.00[CEU][hapmap];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs493152	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs497900	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs500687	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs520904	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs524164	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs531577	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs558905	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs559160	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs564455	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs603723	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs62282169	0.80[EUR][1000 genomes]
rs62282204	0.80[EUR][1000 genomes]
rs624099	0.96[CEU][hapmap];1.00[CHB][hapmap];0.82[YRI][hapmap]
rs635592	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs6439817	0.96[CEU][hapmap];1.00[YRI][hapmap]
rs6439828	0.81[CEU][hapmap]
rs6773514	1.00[CEU][hapmap];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6776585	0.81[EUR][1000 genomes]
rs6780989	0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6784610	0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6791627	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6794270	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6800801	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6801207	0.80[EUR][1000 genomes]
rs6810351	0.81[EUR][1000 genomes]
rs7612106	0.81[EUR][1000 genomes]
rs7613579	1.00[CEU][hapmap];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7628172	0.91[EUR][1000 genomes]
rs7643722	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[YRI][hapmap]
rs7646689	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7650967	1.00[CEU][hapmap];0.92[EUR][1000 genomes]
rs773045	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap]
rs9647336	0.96[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9647337	0.96[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9813576	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9817727	0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9818354	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9821694	0.96[CEU][hapmap];1.00[YRI][hapmap]
rs9822500	0.89[EUR][1000 genomes]
rs9822714	0.96[CEU][hapmap];1.00[CHB][hapmap]
rs9834963	0.96[CEU][hapmap];1.00[CHB][hapmap];0.80[EUR][1000 genomes]
rs9851887	0.84[EUR][1000 genomes]
rs9855727	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9877108	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9879784	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530057	chr3:138014877-138734390	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv1013074	chr3:138213166-138737688	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv1002612	chr3:138213274-138831792	Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
4	nsv536726	chr3:138213274-138831792	Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
5	nsv1009726	chr3:138219923-138737688	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv869205	chr3:138248190-138775288	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv868955	chr3:138248190-138848947	Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
8	nsv591854	chr3:138348081-138764229	Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
9	nsv1010514	chr3:138365640-138737688	Flanking Bivalent TSS/Enh Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
10	nsv1000927	chr3:138423543-138632596	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
11	nsv917964	chr3:138440701-138699084	Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs9289566	CEP70	Cis_1M	lymphoblastoid	RTeQTL
rs9289566	FAIM	cis	Muscle Skeletal	GTEx
rs9289566	PIK3CB	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138551600-138554400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr3:138551800-138554400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:138552200-138554400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
4	chr3:138552200-138554400	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr3:138552400-138554400	Active TSS	H9 Cell Line	embryonic stem cell
6	chr3:138552400-138554400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr3:138552400-138554400	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr3:138552400-138554400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr3:138552400-138554400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr3:138552400-138554400	Active TSS	Breast Myoepithelial Primary Cells	Breast
11	chr3:138552400-138554400	Active TSS	Aorta	Aorta
12	chr3:138552400-138554400	Active TSS	Brain Angular Gyrus	brain
13	chr3:138552400-138554400	Active TSS	Brain Germinal Matrix	brain
14	chr3:138552400-138554400	Active TSS	Left Ventricle	heart
15	chr3:138552400-138554400	Active TSS	Psoas Muscle	Psoas
16	chr3:138552400-138554400	Active TSS	A549	lung
17	chr3:138552600-138554400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr3:138552600-138554400	Active TSS	Esophagus	oesophagus
19	chr3:138552600-138554400	Active TSS	Ovary	ovary
20	chr3:138552600-138554400	Bivalent/Poised TSS	HepG2	liver
21	chr3:138552600-138554600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr3:138552800-138554400	Active TSS	Right Ventricle	heart
23	chr3:138552800-138554600	Active TSS	Fetal Brain Female	brain
24	chr3:138553000-138554800	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr3:138553000-138555000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr3:138553600-138554600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr3:138553600-138554600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr3:138553800-138554400	Flanking Active TSS	Primary B cells from cord blood	blood
29	chr3:138553800-138554400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
30	chr3:138553800-138554600	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
31	chr3:138553800-138554600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr3:138553800-138554600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr3:138554000-138554400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
34	chr3:138554000-138554400	Flanking Active TSS	Primary B cells from peripheral blood	blood
35	chr3:138554000-138554400	Flanking Active TSS	Primary T cells fromperipheralblood	blood
36	chr3:138554000-138554400	Flanking Active TSS	Primary hematopoietic stem cells	blood
37	chr3:138554000-138554400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
38	chr3:138554000-138554400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
39	chr3:138554000-138554400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
40	chr3:138554000-138554400	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
41	chr3:138554000-138554400	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
42	chr3:138554000-138554400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr3:138554000-138554400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr3:138554000-138554400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
45	chr3:138554000-138554400	Flanking Active TSS	Colonic Mucosa	Colon
46	chr3:138554000-138554400	Flanking Active TSS	Fetal Intestine Large	intestine
47	chr3:138554000-138554400	Flanking Active TSS	Placenta	Placenta
48	chr3:138554000-138554400	Flanking Active TSS	Stomach Mucosa	stomach
49	chr3:138554000-138554400	Flanking Active TSS	Thymus	Thymus
50	chr3:138554000-138554400	Flanking Active TSS	HSMM	muscle

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