Variant report

Variant	rs1363907
Chromosome Location	chr5:96252803-96252804
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:96250090..96254054-chr5:96271244..96274355,3	K562	blood:
2	chr5:96251167..96254648-chr5:96255205..96257867,3	K562	blood:

Variant related genes	Relation type
ENSG00000247121	Chromatin interaction

Extended variants
information (count: 126 )
Associated
traits (count: 25 )

rSNPs within LD-proxies of this variant (count:117)

rs_ID	r²[population]
rs10038651	0.85[EUR][1000 genomes]
rs10044354	0.85[CEU][hapmap];0.83[CHD][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes]
rs10051637	0.85[CEU][hapmap];0.83[CHD][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10058476	0.96[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10069361	0.83[CHD][hapmap]
rs10077945	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10434709	0.89[CEU][hapmap]
rs1046395	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1046396	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10476696	0.85[EUR][1000 genomes]
rs11135484	0.89[CEU][hapmap]
rs1216566	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1216567	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1216571	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1230358	0.88[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap]
rs12516666	0.89[CEU][hapmap]
rs13167902	0.89[CEU][hapmap]
rs13170029	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13358339	0.85[EUR][1000 genomes]
rs1363908	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1363974	0.85[CEU][hapmap];0.83[CHD][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.85[EUR][1000 genomes]
rs1363976	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1423357	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs1423566	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1477364	0.96[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1544777	0.96[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.88[YRI][hapmap];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1559355	0.89[CEU][hapmap]
rs18059	0.81[CHD][hapmap];0.82[MEX][hapmap]
rs1820148	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1974871	0.82[ASW][hapmap];0.85[CEU][hapmap];0.82[LWK][hapmap];0.84[YRI][hapmap]
rs2113050	0.84[CEU][hapmap]
rs2161548	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs2247650	0.85[CEU][hapmap]
rs2278018	0.89[CEU][hapmap]
rs2278019	0.89[CEU][hapmap]
rs2351010	0.85[CEU][hapmap];0.83[CHD][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.86[EUR][1000 genomes]
rs2351011	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2432141	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2432142	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs251339	0.85[CEU][hapmap];0.84[CHB][hapmap];0.88[JPT][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs251340	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs251341	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs251343	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2548224	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2548226	0.86[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2548516	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2548527	0.88[ASW][hapmap];0.92[YRI][hapmap]
rs2548529	0.82[CEU][hapmap]
rs2548530	0.96[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2548532	0.92[CEU][hapmap];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2549778	0.88[JPT][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap]
rs2549783	0.96[CEU][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2549784	0.81[CEU][hapmap];0.86[YRI][hapmap]
rs2549791	0.84[YRI][hapmap]
rs2549794	1.00[ASW][hapmap];0.96[CEU][hapmap];0.84[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.97[TSI][hapmap];0.96[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2617435	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2617438	0.88[JPT][hapmap]
rs2617439	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2617447	0.96[CEU][hapmap];0.82[CHB][hapmap];0.94[JPT][hapmap];0.87[YRI][hapmap];0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs27289	0.83[EUR][1000 genomes]
rs27290	0.85[CEU][hapmap];0.80[CHD][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.83[EUR][1000 genomes]
rs27293	0.83[EUR][1000 genomes]
rs27295	0.83[EUR][1000 genomes]
rs27300	0.85[CEU][hapmap];0.83[CHD][hapmap];0.82[MEX][hapmap];0.81[TSI][hapmap]
rs27306	1.00[ASW][hapmap];0.96[CEU][hapmap];0.84[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.97[TSI][hapmap];0.88[EUR][1000 genomes]
rs27307	0.96[CEU][hapmap];0.84[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.88[EUR][1000 genomes]
rs27436	0.81[CEU][hapmap];0.83[EUR][1000 genomes]
rs27613	0.83[CHD][hapmap]
rs2762	0.85[CEU][hapmap];0.82[CHD][hapmap];0.88[TSI][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs27659	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs27660	0.88[EUR][1000 genomes]
rs27711	0.93[ASW][hapmap];0.96[CEU][hapmap];0.84[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];0.88[LWK][hapmap];1.00[MEX][hapmap];0.83[MKK][hapmap];0.97[TSI][hapmap];0.88[EUR][1000 genomes]
rs27712	0.96[CEU][hapmap];0.84[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap];0.86[EUR][1000 genomes]
rs27993	0.93[ASW][hapmap];0.96[CEU][hapmap];0.84[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];0.88[LWK][hapmap];0.83[MKK][hapmap];0.97[TSI][hapmap];0.88[EUR][1000 genomes]
rs2859491	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2910686	0.81[CEU][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2910687	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2910787	0.83[CHD][hapmap]
rs2910788	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2910789	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2910793	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2927608	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2927609	0.96[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3734015	0.89[CEU][hapmap]
rs3797796	0.92[CEU][hapmap];0.86[JPT][hapmap];0.83[EUR][1000 genomes]
rs38029	0.88[EUR][1000 genomes]
rs38031	0.88[EUR][1000 genomes]
rs38032	0.92[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs38033	0.85[CEU][hapmap];0.86[EUR][1000 genomes]
rs38034	0.82[CEU][hapmap];0.82[CHD][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.86[EUR][1000 genomes]
rs38038	0.83[EUR][1000 genomes]
rs38039	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs38040	0.83[CHD][hapmap]
rs38042	0.85[CEU][hapmap]
rs38043	0.85[CEU][hapmap];0.83[EUR][1000 genomes]
rs38044	0.83[EUR][1000 genomes]
rs3849749	0.96[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.96[YRI][hapmap];0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3909451	0.85[CEU][hapmap];0.81[CHD][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes]
rs39602	0.85[CEU][hapmap];0.81[EUR][1000 genomes]
rs4360063	0.84[CEU][hapmap];0.86[EUR][1000 genomes]
rs4869313	0.81[EUR][1000 genomes]
rs4869314	0.89[CEU][hapmap]
rs55770741	0.84[EUR][1000 genomes]
rs6556942	0.92[CEU][hapmap];0.88[JPT][hapmap];0.91[YRI][hapmap];0.84[EUR][1000 genomes]
rs6859168	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6871162	0.85[CEU][hapmap];0.83[CHD][hapmap];1.00[MEX][hapmap];0.90[TSI][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6873866	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs6887500	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs716848	0.96[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7703341	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7716222	0.85[CEU][hapmap];0.83[CHD][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.85[EUR][1000 genomes]
rs7719705	0.96[CEU][hapmap];0.84[CHB][hapmap];0.94[JPT][hapmap];0.87[YRI][hapmap];0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7726445	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7731592	0.85[CEU][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7733312	0.88[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9127	0.92[CEU][hapmap]
rs9314181	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv948703	chr5:96078309-96368839	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
4	nsv1027472	chr5:96081592-96337550	Strong transcription Genic enhancers Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
5	nsv1028741	chr5:96082401-96372165	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
6	nsv949058	chr5:96082433-96390619	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
7	nsv598963	chr5:96084776-96363407	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
8	nsv531967	chr5:96127842-96302702	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
9	nsv823147	chr5:96247723-96257836	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

Variant related diseases (count:1)

Disease	PMID	Source
Inflammatory bowel disease	23128233	GWAS catalog

mRNA abundance (count:24)

SNP	Gene	Cis/trans	Tissue	Source
rs1363907	ERAP2	cis	Artery Aorta	GTEx
rs1363907	ERAP2	cis	Stomach	GTEx
rs1363907	LRAP	Cis_1M	lymphoblastoid	RTeQTL
rs1363907	ERAP2	cis	lymphoblastoid	seeQTL
rs1363907	ERAP2	cis	Esophagus Mucosa	GTEx
rs1363907	LNPEP	cis	parietal	SCAN
rs1363907	AC008865.1	cis	Artery Tibial	GTEx
rs1363907	ERAP2	cis	Artery Tibial	GTEx
rs1363907	LNPEP	cis	Esophagus Muscularis	GTEx
rs1363907	ERAP2	cis	Muscle Skeletal	GTEx
rs1363907	ERAP2	cis	lung	GTEx
rs1363907	ERAP2	cis	lymphoblastoid	GTEx
rs1363907	ERAP2	cis	Thyroid	GTEx
rs1363907	ERAP2	cis	Whole Blood	GTEx
rs1363907	ERAP2	cis	Esophagus Muscularis	GTEx
rs1363907	ERAP2	cis	Skin Sun Exposed Lower leg	GTEx
rs1363907	LRAP	cis	uninvolved skin	skin_eQTL
rs1363907	ERAP2	cis	Heart Left Ventricle	GTEx
rs1363907	ERAP2	cis	parietal	SCAN
rs1363907	ERAP2	cis	Adipose Subcutaneous	GTEx
rs1363907	ERAP2	cis	Nerve Tibial	GTEx
rs1363907	LRAP	cis	normal skin	skin_eQTL
rs1363907	ERAP2	cis	cerebellum	SCAN
rs1363907	LRAP	cis	lesional skin	skin_eQTL

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:96218000-96264600	Weak transcription	Right Ventricle	heart
2	chr5:96218600-96259600	Weak transcription	HMEC	breast
3	chr5:96221600-96269200	Weak transcription	Fetal Brain Male	brain
4	chr5:96222000-96268600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr5:96222400-96258200	Weak transcription	Stomach Mucosa	stomach
6	chr5:96225600-96266400	Weak transcription	Gastric	stomach
7	chr5:96229600-96269600	Weak transcription	Aorta	Aorta
8	chr5:96229800-96256800	Weak transcription	NHEK	skin
9	chr5:96229800-96256800	Weak transcription	Osteobl	bone
10	chr5:96229800-96257000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr5:96229800-96270000	Weak transcription	Esophagus	oesophagus
12	chr5:96232600-96258400	Weak transcription	Brain Hippocampus Middle	brain
13	chr5:96233000-96255600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
14	chr5:96233000-96256200	Strong transcription	Primary T cells fromperipheralblood	blood
15	chr5:96233800-96256000	Strong transcription	Primary B cells from peripheral blood	blood
16	chr5:96234200-96255600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr5:96237400-96269200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:96237800-96265000	Weak transcription	Fetal Muscle Leg	muscle
19	chr5:96238400-96256800	Weak transcription	NHDF-Ad	bronchial
20	chr5:96239400-96256800	Weak transcription	HSMM	muscle
21	chr5:96239400-96257200	Weak transcription	NHLF	lung
22	chr5:96239800-96268000	Weak transcription	Colonic Mucosa	Colon
23	chr5:96240200-96253600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr5:96240400-96254200	Strong transcription	GM12878-XiMat	blood
25	chr5:96240600-96256800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr5:96242000-96259800	Weak transcription	Fetal Stomach	stomach
27	chr5:96242200-96255600	Strong transcription	Primary T helper cells fromperipheralblood	blood
28	chr5:96242200-96256000	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr5:96242200-96268000	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr5:96243400-96257200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr5:96243600-96255000	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
32	chr5:96243600-96266400	Weak transcription	Brain Angular Gyrus	brain
33	chr5:96243800-96256000	Strong transcription	Fetal Thymus	thymus
34	chr5:96244200-96258600	Weak transcription	Brain Cingulate Gyrus	brain
35	chr5:96245200-96256600	Weak transcription	Rectal Smooth Muscle	rectum
36	chr5:96245400-96258200	Weak transcription	Small Intestine	intestine
37	chr5:96245400-96259600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr5:96245400-96259800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
39	chr5:96245600-96255800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr5:96245800-96253600	Weak transcription	Placenta	Placenta
41	chr5:96245800-96254200	Strong transcription	Primary T helper cells PMA-I stimulated	--
42	chr5:96245800-96256600	Weak transcription	HUVEC	blood vessel
43	chr5:96245800-96256800	Weak transcription	Colon Smooth Muscle	Colon
44	chr5:96245800-96258600	Weak transcription	Ovary	ovary
45	chr5:96245800-96264600	Weak transcription	Left Ventricle	heart
46	chr5:96246000-96256800	Weak transcription	Stomach Smooth Muscle	stomach
47	chr5:96246000-96258000	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr5:96246000-96268200	Weak transcription	Fetal Intestine Small	intestine
49	chr5:96246000-96270200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr5:96247400-96258200	Weak transcription	Fetal Lung	lung

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