Variant report

Variant	rs4793842
Chromosome Location	chr17:45671506-45671507
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 104 )
Associated
traits (count: 16 )

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10163469	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10432035	0.81[ASN][1000 genomes]
rs10853090	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11079782	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11079783	0.86[ASW][hapmap];0.95[LWK][hapmap];0.81[TSI][hapmap]
rs11079784	0.87[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.95[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.89[YRI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1138193	0.92[ASN][1000 genomes]
rs11650372	0.89[EUR][1000 genomes]
rs11656855	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11870935	0.84[CEU][hapmap];0.83[GIH][hapmap];0.95[TSI][hapmap];0.87[EUR][1000 genomes]
rs11871606	0.87[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.91[MEX][hapmap];0.83[MKK][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12150231	0.89[EUR][1000 genomes]
rs12452315	0.88[CEU][hapmap];0.91[TSI][hapmap]
rs12603290	0.86[EUR][1000 genomes]
rs12936468	0.87[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12937560	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12943464	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1962307	0.81[TSI][hapmap]
rs2125873	0.83[ASN][1000 genomes]
rs2317826	0.88[CEU][hapmap];0.81[GIH][hapmap];0.95[TSI][hapmap];0.87[EUR][1000 genomes]
rs35919601	0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3760370	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3760371	0.86[ASW][hapmap];0.95[LWK][hapmap];0.81[TSI][hapmap]
rs3809868	0.88[CEU][hapmap];0.83[GIH][hapmap];0.95[TSI][hapmap];0.84[EUR][1000 genomes]
rs3865314	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4092460	0.88[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4239162	0.81[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4239163	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4289035	0.93[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4375701	0.87[EUR][1000 genomes]
rs4399567	0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4580230	0.85[EUR][1000 genomes]
rs4793836	0.84[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs4793908	0.89[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4793913	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4793978	0.87[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.95[MEX][hapmap];0.86[MKK][hapmap];1.00[TSI][hapmap];0.90[YRI][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4794001	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4794016	0.88[EUR][1000 genomes]
rs4794047	0.82[TSI][hapmap]
rs4794048	0.88[CEU][hapmap];0.95[TSI][hapmap]
rs4794058	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap]
rs4794372	0.80[EUR][1000 genomes]
rs55633793	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs55687600	0.81[ASN][1000 genomes]
rs56226803	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62074014	0.83[EUR][1000 genomes]
rs62074015	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6503796	0.81[ASW][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.87[TSI][hapmap];0.84[ASN][1000 genomes]
rs6505048	0.84[AFR][1000 genomes]
rs6505049	0.84[AFR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7207542	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7210472	0.82[EUR][1000 genomes]
rs7210738	0.88[CEU][hapmap];0.83[GIH][hapmap];0.95[TSI][hapmap];0.83[EUR][1000 genomes]
rs7213086	0.94[ASN][1000 genomes]
rs7214799	0.93[ASW][hapmap];0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];0.95[LWK][hapmap];0.87[TSI][hapmap];0.84[YRI][hapmap];0.96[ASN][1000 genomes]
rs7219303	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7220935	0.91[EUR][1000 genomes]
rs7222225	0.86[ASW][hapmap];0.95[LWK][hapmap];0.81[TSI][hapmap]
rs7223029	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73315878	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8065437	0.89[EUR][1000 genomes]
rs8065669	0.88[CEU][hapmap];0.95[TSI][hapmap];0.88[EUR][1000 genomes]
rs8070463	0.81[CEU][hapmap];0.86[CHD][hapmap]
rs8070759	0.87[EUR][1000 genomes]
rs8072100	0.88[CEU][hapmap];0.96[EUR][1000 genomes]
rs8072644	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.91[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs8075411	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8077106	0.86[EUR][1000 genomes]
rs8078686	0.84[CEU][hapmap];0.80[GIH][hapmap];0.84[TSI][hapmap]
rs8078880	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.82[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8081717	0.86[EUR][1000 genomes]
rs8082284	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9635762	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9635763	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9891111	0.96[ASN][1000 genomes]
rs9905583	0.86[EUR][1000 genomes]
rs9905922	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9911944	0.88[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:26 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062983	chr17:45030095-45789543	Strong transcription Active TSS Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv516872	chr17:45419139-45702280	Strong transcription Genic enhancers Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking 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	9 gene(s)	inside rSNPs	diseases
3	nsv525267	chr17:45451894-45735706	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	esv1806110	chr17:45477544-45673592	Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv833468	chr17:45511563-45683164	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv469573	chr17:45511582-45698942	Strong transcription Genic enhancers Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv471701	chr17:45511583-45698942	Genic enhancers Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	esv1811231	chr17:45520374-45764956	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
9	esv1813964	chr17:45520374-45764956	Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	esv2758458	chr17:45520374-45764956	Weak transcription Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
11	esv2758693	chr17:45520374-45764956	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
12	nsv428344	chr17:45520374-45764956	Weak transcription Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
13	nsv908570	chr17:45571502-45684651	Weak transcription Strong transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
14	esv1818529	chr17:45583088-45683095	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
15	nsv471403	chr17:45608444-45700642	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
16	nsv482203	chr17:45608444-45700642	Weak transcription Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
17	esv1811254	chr17:45609466-45673592	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
18	esv1808701	chr17:45610793-45675401	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
19	nsv821341	chr17:45611031-45671632	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
20	nsv828033	chr17:45611031-45671632	Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
21	esv1814312	chr17:45611212-45683095	Strong transcription Enhancers Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
22	nsv9568	chr17:45613661-45672773	Strong transcription Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
23	esv1815163	chr17:45616653-45675272	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
24	esv995713	chr17:45632210-45673517	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers	TF binding region	2 gene(s)	inside rSNPs	diseases
25	esv1851900	chr17:45634373-45673592	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region	2 gene(s)	inside rSNPs	diseases
26	esv1847040	chr17:45635179-45683095	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:16)

SNP	Gene	Cis/trans	Tissue	Source
rs4793842	NPEPPS	cis	parietal	SCAN
rs4793842	TBKBP1	cis	Artery Tibial	GTEx
rs4793842	C17orf57	cis	cerebellum	SCAN
rs4793842	TBKBP1	cis	Nerve Tibial	GTEx
rs4793842	KPNB1	Cis_1M	lymphoblastoid	RTeQTL
rs4793842	RPRML	cis	parietal	SCAN
rs4793842	DBF4B	cis	cerebellum	SCAN
rs4793842	C17orf57	cis	parietal	SCAN
rs4793842	SCRN2	cis	lung	GTEx
rs4793842	RAB5C	cis	parietal	SCAN
rs4793842	TBKBP1	cis	lymphoblastoid	seeQTL
rs4793842	MRPL45P2	cis	lymphoblastoid	seeQTL
rs4793842	VPS25	cis	cerebellum	SCAN
rs4793842	C17orf65	cis	cerebellum	SCAN
rs4793842	VPS25	cis	parietal	SCAN
rs4793842	CDK5RAP3	cis	cerebellum	SCAN

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45610000-45676800	Weak transcription	Ovary	ovary
2	chr17:45610200-45674200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr17:45611200-45674800	Weak transcription	Primary B cells from cord blood	blood
4	chr17:45616600-45674600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr17:45618600-45674600	Weak transcription	Fetal Brain Female	brain
6	chr17:45629800-45673400	Weak transcription	K562	blood
7	chr17:45637800-45678800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr17:45639600-45675000	Weak transcription	Brain Angular Gyrus	brain
9	chr17:45639800-45676800	Weak transcription	Brain Anterior Caudate	brain
10	chr17:45641000-45678000	Weak transcription	Brain Cingulate Gyrus	brain
11	chr17:45641400-45675000	Weak transcription	Primary hematopoietic stem cells	blood
12	chr17:45644200-45675200	Weak transcription	GM12878-XiMat	blood
13	chr17:45644400-45683800	Weak transcription	Spleen	Spleen
14	chr17:45644600-45673400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr17:45644600-45673600	Weak transcription	Hela-S3	cervix
16	chr17:45645000-45673800	Weak transcription	HMEC	breast
17	chr17:45645600-45678200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr17:45647800-45677000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
19	chr17:45647800-45684800	Weak transcription	Gastric	stomach
20	chr17:45649600-45675200	Weak transcription	Right Ventricle	heart
21	chr17:45650000-45673200	Weak transcription	HepG2	liver
22	chr17:45654800-45672800	Weak transcription	NHDF-Ad	bronchial
23	chr17:45657200-45688200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr17:45657800-45678800	Weak transcription	NHEK	skin
25	chr17:45659000-45676800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr17:45659200-45678600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
27	chr17:45659200-45698800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr17:45659600-45675000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr17:45661400-45673400	Weak transcription	Brain Hippocampus Middle	brain
30	chr17:45662600-45689800	Weak transcription	Psoas Muscle	Psoas
31	chr17:45662800-45675800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
32	chr17:45663600-45677200	Weak transcription	Aorta	Aorta
33	chr17:45663800-45702800	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr17:45664000-45677000	Weak transcription	Fetal Lung	lung
35	chr17:45664800-45695000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr17:45665000-45673600	Weak transcription	Fetal Kidney	kidney
37	chr17:45665000-45677200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr17:45665000-45681000	Weak transcription	Pancreatic Islets	Pancreatic Islet
39	chr17:45665400-45671600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
40	chr17:45665600-45671600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr17:45665600-45671800	Strong transcription	Primary monocytes fromperipheralblood	blood
42	chr17:45665600-45673600	Strong transcription	Thymus	Thymus
43	chr17:45665600-45680600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr17:45665600-45686200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr17:45665600-45698200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr17:45665800-45674600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr17:45665800-45677400	Weak transcription	Rectal Smooth Muscle	rectum
48	chr17:45666000-45671800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr17:45666000-45694200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr17:45666200-45678200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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