Variant report

Variant	rs2856237
Chromosome Location	chr3:50158774-50158775
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:50157801..50161419-chr3:50224013..50228566,6	MCF-7	breast:
2	chr3:50157579..50160318-chr3:50233509..50235124,2	MCF-7	breast:
3	chr3:50157617..50159229-chr3:50261958..50264421,2	MCF-7	breast:
4	chr3:50157890..50164898-chr3:50186493..50191745,15	MCF-7	breast:
5	chr3:50158625..50159212-chr3:50263622..50264247,2	K562	blood:
6	chr3:50157879..50160528-chr3:50162974..50166130,4	K562	blood:
7	chr3:50153410..50155870-chr3:50157177..50159023,3	K562	blood:
8	chr3:50158572..50161152-chr3:50232381..50234438,2	MCF-7	breast:
9	chr3:50158688..50160030-chr3:50191274..50192403,3	MCF-7	breast:
10	chr3:50158714..50160101-chr3:50225873..50227682,16	MCF-7	breast:
11	chr3:50158552..50159685-chr3:50226139..50227732,7	K562	blood:
12	chr3:50158102..50159885-chr3:50296008..50298288,2	MCF-7	breast:
13	chr3:50157983..50159948-chr3:50231806..50233770,3	K562	blood:
14	chr3:50157123..50160509-chr3:50182287..50185771,3	MCF-7	breast:
15	chr3:50158689..50159190-chr3:50263373..50264087,2	MCF-7	breast:
16	chr3:50157840..50167526-chr3:50182100..50196634,43	MCF-7	breast:
17	chr3:50157403..50159553-chr3:50273403..50275024,2	K562	blood:
18	chr3:50131320..50133089-chr3:50157321..50159844,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000114353	Chromatin interaction
ENSG00000003756	Chromatin interaction
ENSG00000235016	Chromatin interaction
ENSG00000001617	Chromatin interaction
ENSG00000230454	Chromatin interaction

Extended variants
information (count: 101 )
Associated
traits (count: 19 )

rSNPs within LD-proxies of this variant (count:84)

rs_ID	r²[population]
rs1046956	0.82[YRI][hapmap]
rs1061474	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11130233	0.89[JPT][hapmap]
rs1138536	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12107768	0.88[ASN][1000 genomes]
rs12496973	0.90[CHD][hapmap]
rs12632110	0.80[YRI][hapmap]
rs12634780	0.92[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs12637671	0.80[YRI][hapmap]
rs13060128	0.90[CHD][hapmap]
rs13067082	0.80[YRI][hapmap]
rs17657664	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs17657688	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs2013208	0.90[CHD][hapmap]
rs2189691	0.80[YRI][hapmap]
rs2240326	0.90[CHD][hapmap]
rs2240327	0.90[CHD][hapmap]
rs2240328	1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[GIH][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs2240329	0.90[CHD][hapmap]
rs2247510	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];0.98[LWK][hapmap];0.93[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2252833	0.90[CHD][hapmap]
rs2301166	0.81[JPT][hapmap]
rs2352969	1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[GIH][hapmap];0.90[JPT][hapmap]
rs2526392	0.89[JPT][hapmap]
rs2526393	0.89[JPT][hapmap]
rs2526394	0.89[JPT][hapmap]
rs2526395	0.89[JPT][hapmap]
rs2526396	0.89[JPT][hapmap]
rs2526747	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2526748	0.90[CHD][hapmap]
rs2526749	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2526750	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2526751	0.90[CHD][hapmap]
rs2526754	0.90[CHD][hapmap]
rs2624815	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2624817	0.91[ASN][1000 genomes]
rs2624819	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap]
rs2624821	1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[GIH][hapmap];0.90[JPT][hapmap]
rs2624822	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2624826	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2624829	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2624834	1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[GIH][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs2624837	0.89[JPT][hapmap]
rs2624842	0.89[JPT][hapmap]
rs2624843	0.90[CHD][hapmap]
rs2624848	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2624853	0.90[CHD][hapmap]
rs2681779	1.00[CHB][hapmap];0.94[CHD][hapmap];0.82[GIH][hapmap];0.90[JPT][hapmap]
rs2856234	0.90[CHD][hapmap];0.81[JPT][hapmap]
rs2856238	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2883057	0.90[CHD][hapmap]
rs3774734	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4688688	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs4688689	0.90[CHD][hapmap]
rs4688690	0.90[CHD][hapmap]
rs4688753	0.96[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4688754	0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4688755	0.90[CHD][hapmap]
rs4688758	0.90[CHD][hapmap]
rs6446193	0.90[CHD][hapmap]
rs6446194	0.84[ASN][1000 genomes]
rs6446195	0.80[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6446197	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6762477	0.92[CEU][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];0.93[TSI][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6765484	0.90[CHD][hapmap]
rs6771546	0.90[CHD][hapmap]
rs6772095	0.90[CHD][hapmap]
rs6774354	1.00[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.94[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap]
rs6778802	0.82[ASN][1000 genomes]
rs6792892	0.90[CHD][hapmap]
rs6793528	0.96[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6799579	0.88[ASN][1000 genomes]
rs6808044	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7061	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7430334	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.95[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7613875	0.90[CHD][hapmap]
rs7621026	0.90[CHD][hapmap]
rs7628058	0.90[CHD][hapmap]
rs7634441	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9311446	0.90[CHD][hapmap]
rs9682295	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9814664	0.90[CHD][hapmap]
rs9861216	0.90[CHD][hapmap]
rs9866695	0.90[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834690	chr3:50101835-50267584	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv515986	chr3:50104307-50267584	Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv432418	chr3:50114496-50224196	Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
4	nsv1001775	chr3:50129479-50311666	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
5	nsv818139	chr3:50144951-50174572	Weak transcription Strong transcription Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases
6	nsv876768	chr3:50144951-50267584	Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Weak transcription Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
7	nsv523662	chr3:50144951-50584999	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
8	nsv1013949	chr3:50151712-50339163	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
9	nsv590250	chr3:50153356-50332697	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
10	nsv876769	chr3:50155468-50408398	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription 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 miRNA target site	94 gene(s)	inside rSNPs	diseases
11	esv1821728	chr3:50156142-50657253	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
12	esv3386929	chr3:50156348-50161346	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
13	esv1793751	chr3:50157364-50476363	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
14	esv1828162	chr3:50157364-50506151	Enhancers Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
15	nsv590251	chr3:50158774-50337422	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
16	nsv470561	chr3:50158774-50584999	Flanking Active TSS Enhancers Weak transcription Genic enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
17	nsv876770	chr3:50158774-50609624	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	103 gene(s)	inside rSNPs	diseases

mRNA abundance (count:19)

SNP	Gene	Cis/trans	Tissue	Source
rs2856237	ARIH2	cis	cerebellum	SCAN
rs2856237	RBM6	cis	Whole Blood	GTEx
rs2856237	RBM6	Cis_1M	lymphoblastoid	RTeQTL
rs2856237	RBM6	cis	Thyroid	GTEx
rs2856237	RBM6	cis	Skin Sun Exposed Lower leg	GTEx
rs2856237	RBM6	cis	Heart Left Ventricle	GTEx
rs2856237	RNF123	cis	parietal	SCAN
rs2856237	RBM6	cis	Adipose Subcutaneous	GTEx
rs2856237	RBM6	cis	cerebellum	SCAN
rs2856237	RNF123	cis	cerebellum	SCAN
rs2856237	QRICH1	cis	cerebellum	SCAN
rs2856237	RBM6	cis	lymphoblastoid	seeQTL
rs2856237	RBM6	cis	Esophagus Mucosa	GTEx
rs2856237	RBM6	cis	parietal	SCAN
rs2856237	RBM6	cis	Artery Aorta	GTEx
rs2856237	RBM6	cis	lung	GTEx
rs2856237	RBM6	cis	Esophagus Muscularis	GTEx
rs2856237	RBM6	cis	Nerve Tibial	GTEx
rs2856237	RBM6	cis	Artery Tibial	GTEx

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:50128200-50158800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:50128400-50159000	Strong transcription	Lung	lung
3	chr3:50128600-50158800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr3:50128600-50158800	Strong transcription	Brain Germinal Matrix	brain
5	chr3:50128600-50158800	Strong transcription	Placenta Amnion	Placenta Amnion
6	chr3:50128600-50159000	Strong transcription	Brain Angular Gyrus	brain
7	chr3:50128600-50159000	Strong transcription	Placenta	Placenta
8	chr3:50128600-50159000	Strong transcription	Sigmoid Colon	Sigmoid Colon
9	chr3:50128600-50159200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:50128600-50159200	Strong transcription	Liver	Liver
11	chr3:50128600-50159200	Strong transcription	NHEK	skin
12	chr3:50128600-50160400	Strong transcription	Fetal Thymus	thymus
13	chr3:50128800-50159000	Strong transcription	Brain Anterior Caudate	brain
14	chr3:50129000-50158800	Strong transcription	Fetal Intestine Large	intestine
15	chr3:50129000-50159000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
16	chr3:50129000-50159200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr3:50129000-50159200	Strong transcription	Primary B cells from peripheral blood	blood
18	chr3:50129000-50159400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr3:50129000-50159400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
20	chr3:50129000-50160000	Strong transcription	Fetal Stomach	stomach
21	chr3:50129000-50160000	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr3:50129000-50160800	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr3:50129200-50158800	Strong transcription	Primary B cells from cord blood	blood
24	chr3:50129200-50158800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr3:50129200-50158800	Strong transcription	Brain Hippocampus Middle	brain
26	chr3:50129200-50159000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:50129200-50159600	Strong transcription	Stomach Smooth Muscle	stomach
28	chr3:50129200-50160000	Strong transcription	Primary monocytes fromperipheralblood	blood
29	chr3:50129200-50160200	Strong transcription	Fetal Brain Female	brain
30	chr3:50129400-50158800	Strong transcription	Pancreas	Pancrea
31	chr3:50129400-50159400	Strong transcription	Spleen	Spleen
32	chr3:50129600-50159200	Strong transcription	Primary T cells from cord blood	blood
33	chr3:50129600-50161600	Strong transcription	Thymus	Thymus
34	chr3:50130000-50159200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr3:50130400-50159800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
36	chr3:50131400-50159600	Strong transcription	Dnd41	blood
37	chr3:50132400-50159000	Strong transcription	Primary T helper cells fromperipheralblood	blood
38	chr3:50133200-50159200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr3:50133200-50159200	Strong transcription	Rectal Mucosa Donor 31	rectum
40	chr3:50133800-50161200	Strong transcription	Right Ventricle	heart
41	chr3:50134000-50159400	Strong transcription	Muscle Satellite Cultured Cells	--
42	chr3:50134400-50158800	Strong transcription	Primary T helper cells PMA-I stimulated	--
43	chr3:50136000-50158800	Strong transcription	Brain Cingulate Gyrus	brain
44	chr3:50136000-50159200	Strong transcription	Rectal Smooth Muscle	rectum
45	chr3:50136200-50159000	Strong transcription	Esophagus	oesophagus
46	chr3:50138000-50159800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:50138800-50159600	Strong transcription	NHLF	lung
48	chr3:50139000-50158800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr3:50139200-50159800	Strong transcription	HSMM	muscle
50	chr3:50139400-50158800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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