Variant report

Variant	rs2302415
Chromosome Location	chr17:15906391-15906392
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 124 )
Associated
traits (count: 18 )

rSNPs within LD-proxies of this variant (count:106)

rs_ID	r²[population]
rs1045599	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.94[JPT][hapmap];0.87[MEX][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1065822	0.82[CEU][hapmap]
rs1075901	0.92[CEU][hapmap];0.85[CHB][hapmap];0.84[CHD][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1079533	0.82[CEU][hapmap]
rs11078320	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11078327	0.84[EUR][1000 genomes]
rs11078331	0.83[EUR][1000 genomes]
rs1125156	0.81[CEU][hapmap]
rs1160109	0.82[CEU][hapmap]
rs11650678	0.82[CEU][hapmap]
rs11651290	0.82[CEU][hapmap]
rs11652025	0.84[EUR][1000 genomes]
rs11654	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11655456	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11656046	0.85[EUR][1000 genomes]
rs11657160	0.96[CEU][hapmap];0.85[CHB][hapmap];0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11869450	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[CHD][hapmap];1.00[GIH][hapmap];0.88[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11869563	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.96[MEX][hapmap];0.86[MKK][hapmap];0.98[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11872032	0.82[CEU][hapmap]
rs12945463	0.82[EUR][1000 genomes]
rs178657	0.82[CEU][hapmap]
rs178805	0.81[CEU][hapmap]
rs178809	0.82[CEU][hapmap]
rs178814	0.96[CEU][hapmap];0.85[CHB][hapmap]
rs178815	0.96[CEU][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap]
rs178816	0.82[CEU][hapmap]
rs178820	0.82[CEU][hapmap]
rs178822	0.96[CEU][hapmap];0.85[CHB][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap]
rs178838	0.96[CEU][hapmap];0.85[CHB][hapmap]
rs178839	0.96[CEU][hapmap]
rs1860643	0.90[ASN][1000 genomes]
rs1860644	0.88[ASN][1000 genomes]
rs1860645	0.88[ASN][1000 genomes]
rs1989856	0.82[CEU][hapmap]
rs2015353	0.87[MEX][hapmap];0.84[TSI][hapmap]
rs2078050	0.96[CEU][hapmap];0.85[CHB][hapmap];0.81[CHD][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes]
rs2109632	0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2157990	0.93[CEU][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes]
rs2157991	0.96[CEU][hapmap];0.85[CHB][hapmap];0.81[CHD][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.85[EUR][1000 genomes]
rs2157992	0.82[CEU][hapmap]
rs2159643	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2285582	0.85[EUR][1000 genomes]
rs2285583	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2286795	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2286796	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2324141	0.96[CEU][hapmap];0.85[CHB][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap]
rs2324142	0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs2535614	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2779207	0.87[ASN][1000 genomes]
rs2779208	0.87[ASN][1000 genomes]
rs2779210	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2779212	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.91[TSI][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs35168566	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3760297	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3785628	0.96[CEU][hapmap];0.85[CHB][hapmap];0.81[CHD][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.85[EUR][1000 genomes]
rs3785629	0.84[EUR][1000 genomes]
rs3785631	0.82[CEU][hapmap]
rs3785632	0.85[CEU][hapmap];0.85[TSI][hapmap]
rs3785633	0.82[CEU][hapmap]
rs3815039	0.82[CEU][hapmap]
rs3826360	0.82[CEU][hapmap]
rs4435297	0.92[CEU][hapmap];0.85[CHB][hapmap];0.81[CHD][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap];0.85[EUR][1000 genomes]
rs4791662	0.82[CEU][hapmap]
rs4792707	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4792708	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4792709	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4792712	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4792713	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4792715	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4792716	0.80[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4792717	0.96[CEU][hapmap];0.85[CHB][hapmap];0.85[EUR][1000 genomes]
rs4792718	1.00[ASW][hapmap];1.00[CEU][hapmap];0.93[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.96[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4792721	0.81[CEU][hapmap];0.84[TSI][hapmap]
rs6416868	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6502479	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6502480	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6502482	0.96[CEU][hapmap];0.85[CHB][hapmap];0.87[EUR][1000 genomes]
rs6502488	0.96[CEU][hapmap];0.85[CHB][hapmap];0.84[CHD][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.85[EUR][1000 genomes]
rs7209094	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7210655	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7214695	0.96[CEU][hapmap];0.85[CHB][hapmap]
rs7216949	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7223346	0.96[CEU][hapmap];0.85[CHB][hapmap];0.81[CHD][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap];0.82[EUR][1000 genomes]
rs8064702	0.82[EUR][1000 genomes]
rs8065190	0.85[EUR][1000 genomes]
rs8070859	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.94[LWK][hapmap];0.96[MEX][hapmap];0.86[MKK][hapmap];0.98[TSI][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8075345	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs8076669	0.85[EUR][1000 genomes]
rs8076864	0.85[CEU][hapmap]
rs8079969	0.96[CEU][hapmap];0.85[CHB][hapmap];0.96[MEX][hapmap];0.93[TSI][hapmap]
rs8080221	0.84[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8081406	0.84[EUR][1000 genomes]
rs8081667	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9652827	0.85[EUR][1000 genomes]
rs9709250	0.85[EUR][1000 genomes]
rs9890012	0.82[CEU][hapmap]
rs9891379	0.82[CEU][hapmap]
rs9891938	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[TSI][hapmap];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9896441	0.83[EUR][1000 genomes]
rs9897542	0.88[EUR][1000 genomes]
rs9899002	0.82[CEU][hapmap]
rs9899995	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9902141	0.81[CEU][hapmap]
rs9908031	0.85[CEU][hapmap]
rs9909697	0.82[CEU][hapmap]
rs9916868	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv934185	chr17:15552960-16551197	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	190 gene(s)	inside rSNPs	diseases
2	nsv1066023	chr17:15607267-16053512	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	esv3330182	chr17:15652014-16569534	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
4	esv3446844	chr17:15654843-16572246	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	177 gene(s)	inside rSNPs	diseases
5	nsv1061222	chr17:15672934-15999778	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
6	nsv907706	chr17:15731923-16056442	ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
7	nsv1067555	chr17:15804228-16001117	Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
8	nsv1063459	chr17:15804228-16543593	Weak transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Strong transcription Active TSS 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 miRNA target site	164 gene(s)	inside rSNPs	diseases
9	nsv907707	chr17:15846535-15950751	Strong transcription Weak transcription Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	nsv907709	chr17:15851196-15937487	Weak transcription Genic enhancers Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
11	nsv907708	chr17:15851196-15950751	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
12	nsv1057493	chr17:15852125-15930718	Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
13	nsv543215	chr17:15852125-15930718	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
14	nsv907710	chr17:15854257-15950751	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
15	nsv1062220	chr17:15869557-16093156	Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
16	nsv1064878	chr17:15869557-16097241	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
17	nsv1055173	chr17:15875935-16097241	Flanking Active TSS Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
18	nsv1056157	chr17:15890584-16088473	Strong transcription Genic enhancers Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

mRNA abundance (count:18)

SNP	Gene	Cis/trans	Tissue	Source
rs2302415	TTC19	cis	lymphoblastoid	seeQTL
rs2302415	CENPV	cis	Artery Tibial	GTEx
rs2302415	TTC19	Cis_1M	lymphoblastoid	RTeQTL
rs2302415	ADORA2B	cis	Artery Tibial	GTEx
rs2302415	Hs.379903	cis	multi-tissue	Pritchard
rs2302415	ADORA2B	cis	Nerve Tibial	GTEx
rs2302415	NCOR1	cis	parietal	SCAN
rs2302415	ADORA2B	cis	Muscle Skeletal	GTEx
rs2302415	ADORA2B	cis	Esophagus Muscularis	GTEx
rs2302415	ELAC2	cis	parietal	SCAN
rs2302415	PRPSAP2	cis	parietal	SCAN
rs2302415	ADORA2B	cis	Thyroid	GTEx
rs2302415	ADORA2B	cis	lung	GTEx
rs2302415	ADORA2B	cis	Heart Left Ventricle	GTEx
rs2302415	ADORA2B	cis	Adipose Subcutaneous	GTEx
rs2302415	ZSWIM7	Cis_1M	lymphoblastoid	RTeQTL
rs2302415	CENPV	cis	parietal	SCAN
rs2302415	ZSWIM7	cis	Muscle Skeletal	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15903800-15907000	Weak transcription	Aorta	Aorta
2	chr17:15904000-15910800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr17:15904200-15907400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr17:15904400-15906400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr17:15904400-15906600	Genic enhancers	Left Ventricle	heart
6	chr17:15904400-15912600	Strong transcription	Fetal Muscle Trunk	muscle
7	chr17:15904600-15906600	ZNF genes & repeats	A549	lung
8	chr17:15904600-15912200	Strong transcription	Primary B cells from cord blood	blood
9	chr17:15904600-15912600	Strong transcription	H9 Cell Line	embryonic stem cell
10	chr17:15904600-15913400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr17:15904800-15906400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr17:15904800-15906400	ZNF genes & repeats	GM12878-XiMat	blood
13	chr17:15904800-15906400	Genic enhancers	HepG2	liver
14	chr17:15904800-15906800	ZNF genes & repeats	Fetal Intestine Small	intestine
15	chr17:15904800-15907000	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr17:15904800-15908000	Weak transcription	Right Ventricle	heart
17	chr17:15904800-15909400	Strong transcription	Fetal Kidney	kidney
18	chr17:15904800-15912000	Strong transcription	Fetal Brain Female	brain
19	chr17:15904800-15912400	Strong transcription	Fetal Thymus	thymus
20	chr17:15904800-15912600	Strong transcription	Colon Smooth Muscle	Colon
21	chr17:15904800-15912600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr17:15904800-15912600	Strong transcription	Fetal Lung	lung
23	chr17:15904800-15912600	Strong transcription	Rectal Mucosa Donor 29	rectum
24	chr17:15904800-15914400	Strong transcription	Liver	Liver
25	chr17:15904800-15915800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr17:15904800-15917200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr17:15905000-15907200	Weak transcription	Fetal Brain Male	brain
28	chr17:15905000-15908800	Strong transcription	Ovary	ovary
29	chr17:15905000-15909200	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr17:15905000-15909400	Strong transcription	Pancreas	Pancrea
31	chr17:15905000-15912200	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr17:15905000-15912200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
33	chr17:15905000-15912200	Strong transcription	Brain Substantia Nigra	brain
34	chr17:15905000-15912200	Strong transcription	Colonic Mucosa	Colon
35	chr17:15905000-15912200	Strong transcription	Fetal Muscle Leg	muscle
36	chr17:15905000-15912200	Strong transcription	Fetal Stomach	stomach
37	chr17:15905000-15912600	Strong transcription	Brain Angular Gyrus	brain
38	chr17:15905000-15912600	Strong transcription	Skeletal Muscle Male	skeletal muscle
39	chr17:15905000-15912600	Strong transcription	Skeletal Muscle Female	skeletal muscle
40	chr17:15905000-15912600	Strong transcription	Stomach Smooth Muscle	stomach
41	chr17:15905000-15912600	Strong transcription	Monocytes-CD14+_RO01746	blood
42	chr17:15905000-15913200	Strong transcription	NHDF-Ad	bronchial
43	chr17:15905000-15914600	Weak transcription	Stomach Mucosa	stomach
44	chr17:15905000-15915000	Strong transcription	Muscle Satellite Cultured Cells	--
45	chr17:15905000-15915200	Strong transcription	HSMM	muscle
46	chr17:15905000-15915600	Strong transcription	NH-A	brain
47	chr17:15905000-15915800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr17:15905000-15916000	Strong transcription	Osteobl	bone
49	chr17:15905000-15916800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr17:15905000-15939600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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