Variant report

Variant	rs8032433
Chromosome Location	chr15:62284101-62284102
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	chr15:62283890..62286224-chr15:62350363..62353063,2	K562	blood:

Variant related genes	Relation type
ENSG00000129003	Chromatin interaction
ENSG00000259251	Chromatin interaction

Extended variants
information (count: 110 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs10047986	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1030859	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10468026	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11071642	0.81[CEU][hapmap]
rs11071649	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11629596	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11633500	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11635977	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11638793	0.80[CHB][hapmap];0.81[JPT][hapmap];0.84[MEX][hapmap];0.92[YRI][hapmap]
rs11639482	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12438690	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12438803	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12439356	0.88[CEU][hapmap];0.85[JPT][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12442212	0.88[CEU][hapmap];0.85[JPT][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12442448	0.80[CHB][hapmap];0.81[JPT][hapmap];0.84[MEX][hapmap]
rs12442675	0.92[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.88[TSI][hapmap];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12591155	0.80[CHB][hapmap];0.81[JPT][hapmap]
rs12592402	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12593844	0.91[GIH][hapmap]
rs12594658	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12594946	0.90[AMR][1000 genomes]
rs12899801	0.91[GIH][hapmap]
rs12900645	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12908182	0.82[EUR][1000 genomes]
rs12910541	0.81[CEU][hapmap];0.86[EUR][1000 genomes]
rs12912208	0.81[CEU][hapmap];0.91[GIH][hapmap];0.87[MEX][hapmap];0.80[EUR][1000 genomes]
rs12913951	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12916052	0.82[ASN][1000 genomes]
rs1344601	0.96[CEU][hapmap];0.84[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1436958	1.00[CHB][hapmap];0.89[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.81[TSI][hapmap];0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1436959	0.81[JPT][hapmap]
rs1436963	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1436964	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1436966	0.81[CEU][hapmap];0.93[GIH][hapmap];0.84[MEX][hapmap]
rs1534542	0.84[CHB][hapmap];0.95[JPT][hapmap]
rs17205407	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17205463	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs17271340	0.81[CEU][hapmap]
rs17271403	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs17271438	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2162062	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2414753	0.81[CEU][hapmap]
rs2414754	0.81[CEU][hapmap]
rs28542204	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28837073	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2899677	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs34096515	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34138933	0.89[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs35123892	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3784633	1.00[CEU][hapmap];0.86[CHB][hapmap];0.87[JPT][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3784634	0.85[CEU][hapmap];0.87[TSI][hapmap];0.81[EUR][1000 genomes]
rs4143842	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4143843	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4564516	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4774427	0.81[CEU][hapmap];0.85[TSI][hapmap]
rs4775455	0.92[CEU][hapmap];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4775457	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4775458	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62007368	0.93[AMR][1000 genomes];0.83[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7162536	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7172967	0.81[CEU][hapmap];0.87[TSI][hapmap]
rs7177276	0.88[CEU][hapmap];0.85[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7177711	0.88[CEU][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7178424	0.88[CEU][hapmap];0.85[JPT][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7178540	0.88[CEU][hapmap];0.95[GIH][hapmap];0.85[JPT][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7178945	0.87[CEU][hapmap];0.84[JPT][hapmap];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs731820	0.88[CEU][hapmap];0.95[GIH][hapmap];0.85[JPT][hapmap];0.96[MEX][hapmap];0.88[TSI][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8025877	0.88[CEU][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8026008	0.88[CEU][hapmap];0.84[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8029942	0.81[CEU][hapmap];0.91[GIH][hapmap];0.88[MEX][hapmap];0.81[EUR][1000 genomes]
rs8033816	0.89[GIH][hapmap]
rs8034216	0.81[CEU][hapmap];0.88[TSI][hapmap];0.84[EUR][1000 genomes]
rs8034335	0.81[CEU][hapmap];0.90[TSI][hapmap];0.85[EUR][1000 genomes]
rs8038932	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs8039105	0.81[CEU][hapmap]
rs8039651	0.92[CEU][hapmap];0.84[CHB][hapmap];0.89[CHD][hapmap];0.98[GIH][hapmap];0.95[JPT][hapmap];0.95[MEX][hapmap];0.90[TSI][hapmap];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs893156	0.88[CEU][hapmap];0.90[JPT][hapmap];0.84[YRI][hapmap];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs893158	0.88[CEU][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs933807	1.00[ASW][hapmap];0.96[CEU][hapmap];0.81[CHD][hapmap];0.98[GIH][hapmap];0.90[JPT][hapmap];1.00[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9920758	0.80[CHB][hapmap];0.81[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521334	chr15:62129809-62340126	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv527451	chr15:62129809-62340126	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv904286	chr15:62146598-62313373	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
4	nsv904287	chr15:62146598-62338797	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
5	nsv904288	chr15:62146598-62356386	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
6	nsv569641	chr15:62155282-62287456	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	nsv904289	chr15:62156690-62287456	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	nsv516639	chr15:62175134-62340126	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv904290	chr15:62175134-62356386	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
10	nsv904291	chr15:62178695-62287456	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv904292	chr15:62178695-62313373	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv904293	chr15:62178695-62338797	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv904294	chr15:62178695-62356386	Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	nsv457176	chr15:62178695-62519658	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
15	nsv569643	chr15:62178695-62519658	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
16	nsv904296	chr15:62198564-62313373	ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
17	nsv471247	chr15:62202481-62519658	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
18	nsv904297	chr15:62202482-62313373	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
19	nsv569645	chr15:62202482-62319307	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
20	nsv569646	chr15:62202482-62519658	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
21	esv1816724	chr15:62205104-62285146	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
22	nsv569647	chr15:62214607-62284101	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
23	nsv904298	chr15:62218689-62338797	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
24	nsv569648	chr15:62239697-62340126	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
25	nsv457177	chr15:62243197-62301094	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
26	nsv569649	chr15:62243197-62301094	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
27	nsv569650	chr15:62243197-62313373	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
28	nsv569651	chr15:62243197-62313417	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
29	nsv1044748	chr15:62276183-62521856	Active TSS Enhancers Bivalent/Poised TSS Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
30	nsv542405	chr15:62276183-62521856	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs8032433	TEX9	cis	parietal	SCAN
rs8032433	USP3	cis	cerebellum	SCAN
rs8032433	VPS13C	cis	cerebellum	SCAN

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:62185600-62333600	Weak transcription	Right Ventricle	heart
2	chr15:62185800-62300000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr15:62188600-62309400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr15:62195600-62285400	Strong transcription	Primary monocytes fromperipheralblood	blood
5	chr15:62208200-62290200	Weak transcription	Aorta	Aorta
6	chr15:62221400-62327600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr15:62230800-62317200	Weak transcription	Pancreas	Pancrea
8	chr15:62235800-62285000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr15:62244600-62350400	Weak transcription	Small Intestine	intestine
10	chr15:62254000-62303600	Weak transcription	Spleen	Spleen
11	chr15:62254200-62287800	Weak transcription	Lung	lung
12	chr15:62254200-62297800	Weak transcription	Fetal Intestine Small	intestine
13	chr15:62259400-62327200	Weak transcription	HepG2	liver
14	chr15:62262600-62312600	Weak transcription	NHEK	skin
15	chr15:62263800-62287800	Weak transcription	Fetal Stomach	stomach
16	chr15:62263800-62290200	Weak transcription	Gastric	stomach
17	chr15:62264000-62287000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr15:62264000-62312600	Weak transcription	Rectal Smooth Muscle	rectum
19	chr15:62264000-62323800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr15:62264000-62324000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
21	chr15:62264800-62286200	Weak transcription	Osteobl	bone
22	chr15:62264800-62299400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr15:62265000-62299400	Weak transcription	Brain Germinal Matrix	brain
24	chr15:62265000-62299800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr15:62265600-62299600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr15:62265600-62338200	Weak transcription	Stomach Mucosa	stomach
27	chr15:62265800-62299200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr15:62266000-62299200	Weak transcription	Fetal Kidney	kidney
29	chr15:62267200-62285400	Strong transcription	Monocytes-CD14+_RO01746	blood
30	chr15:62267400-62287800	Weak transcription	Brain Hippocampus Middle	brain
31	chr15:62267600-62285200	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr15:62267600-62299800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr15:62271200-62299200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr15:62271600-62297800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr15:62273600-62300400	Weak transcription	Fetal Muscle Trunk	muscle
36	chr15:62274800-62288000	Weak transcription	Brain Cingulate Gyrus	brain
37	chr15:62274800-62299000	Weak transcription	NH-A	brain
38	chr15:62276400-62299000	Weak transcription	HSMMtube	muscle
39	chr15:62276400-62299200	Weak transcription	Hela-S3	cervix
40	chr15:62276400-62299400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
41	chr15:62276400-62326800	Weak transcription	Thymus	Thymus
42	chr15:62276400-62345000	Weak transcription	Colon Smooth Muscle	Colon
43	chr15:62276600-62288000	Weak transcription	Brain Angular Gyrus	brain
44	chr15:62276600-62289600	Weak transcription	Left Ventricle	heart
45	chr15:62276600-62299800	Weak transcription	Fetal Muscle Leg	muscle
46	chr15:62276600-62299800	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr15:62276600-62327600	Weak transcription	NHLF	lung
48	chr15:62276800-62288000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr15:62276800-62288000	Weak transcription	Brain Inferior Temporal Lobe	brain
50	chr15:62276800-62288400	Weak transcription	HMEC	breast

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