Variant report

Variant	rs10491104
Chromosome Location	chr17:15884561-15884562
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr17:15884411-15884928	GM12878	blood:	n/a	n/a
2	STAT5A	chr17:15884528-15884821	GM12878	blood:	n/a	chr17:15884626-15884638
3	RUNX3	chr17:15884406-15884914	GM12878	blood:	n/a	chr17:15884703-15884720
4	FOXM1	chr17:15884373-15884899	GM12878	blood:	n/a	n/a
5	ATF2	chr17:15884539-15884890	GM12878	blood:	n/a	n/a
6	WRNIP1	chr17:15884410-15885034	GM12878	blood:	n/a	n/a
7	EP300	chr17:15884519-15884880	GM12878	blood:	n/a	chr17:15884773-15884782
8	POU2F2	chr17:15884546-15884830	GM12891	blood:	n/a	n/a
9	SPI1	chr17:15884269-15885020	GM12878	blood:	n/a	n/a
10	TBL1XR1	chr17:15884475-15884863	GM12878	blood:	n/a	n/a
11	SPI1	chr17:15884419-15884867	HL-60	blood:	n/a	n/a
12	BCL11A	chr17:15884533-15884893	GM12878	blood:	n/a	n/a
13	RCOR1	chr17:15884479-15884715	K562	blood:	n/a	n/a
14	EBF1	chr17:15883767-15884802	GM12878	blood:	n/a	n/a
15	MTA3	chr17:15884406-15884947	GM12878	blood:	n/a	n/a
16	RCOR1	chr17:15884383-15884885	GM12878	blood:	n/a	n/a
17	SPI1	chr17:15884383-15884954	GM12891	blood:	n/a	n/a
18	STAT5A	chr17:15884448-15884920	GM12878	blood:	n/a	chr17:15884626-15884638
19	NFIC	chr17:15884428-15884954	GM12878	blood:	n/a	n/a
20	NFIC	chr17:15884419-15885010	GM12878	blood:	n/a	n/a
21	SP1	chr17:15884200-15885051	HCT-116	colon:	n/a	n/a
22	SPI1	chr17:15884419-15884956	GM12891	blood:	n/a	n/a
23	MAZ	chr17:15884345-15884946	GM12878	blood:	n/a	chr17:15884781-15884791
24	RUNX3	chr17:15884282-15884977	GM12878	blood:	n/a	chr17:15884286-15884295 chr17:15884703-15884720 chr17:15884286-15884295
25	UBTF	chr17:15884506-15884687	K562	blood:	n/a	n/a
26	SPI1	chr17:15884487-15884836	GM12878	blood:	n/a	n/a
27	NFATC1	chr17:15884478-15884847	GM12878	blood:	n/a	n/a
28	BCL11A	chr17:15884558-15884812	GM12878	blood:	n/a	n/a
29	BATF	chr17:15884479-15884852	GM12878	blood:	n/a	n/a
30	EP300	chr17:15884478-15884868	GM12878	blood:	n/a	chr17:15884773-15884782

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:15884378..15885886-chr17:15892555..15894093,2	K562	blood:
2	chr17:15884386..15887034-chr17:15891736..15894055,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ADORA2B-1	chr17:15884512-15885318	predAs_engstrom06_BC031588_1

Variant related genes	Relation type
ZSWIM7	TF binding region

Extended variants
information (count: 105 )
Associated
traits (count: 22 )

rSNPs within LD-proxies of this variant (count:87)

rs_ID	r²[population]
rs1065822	0.92[CEU][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1075901	0.84[JPT][hapmap]
rs1079533	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.93[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11078321	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11078328	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11078330	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1125156	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes]
rs1160109	0.92[CEU][hapmap]
rs11650678	0.92[CEU][hapmap]
rs11651290	0.92[CEU][hapmap];0.90[CHB][hapmap];0.95[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.93[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11651508	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11657160	0.85[JPT][hapmap]
rs11657912	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11868809	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11869563	0.80[EUR][1000 genomes]
rs11871961	0.83[EUR][1000 genomes]
rs11872032	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12451075	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12942295	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12945546	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12947205	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12948361	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs178657	0.92[CEU][hapmap];0.82[MEX][hapmap];0.89[TSI][hapmap]
rs178837	0.85[CEU][hapmap];0.82[MEX][hapmap];0.87[TSI][hapmap]
rs178838	0.85[JPT][hapmap]
rs1989856	0.92[CEU][hapmap];0.82[MEX][hapmap];0.89[TSI][hapmap]
rs2015353	0.96[CEU][hapmap];0.81[GIH][hapmap];0.92[JPT][hapmap];0.81[TSI][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2041459	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2041460	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2051736	0.91[EUR][1000 genomes]
rs2078050	0.85[JPT][hapmap]
rs2157990	0.92[JPT][hapmap]
rs2157991	0.85[JPT][hapmap]
rs2157992	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2286796	0.80[EUR][1000 genomes]
rs2301652	0.82[TSI][hapmap]
rs2324084	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2324141	0.85[JPT][hapmap]
rs2324142	0.85[JPT][hapmap]
rs2779211	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34236618	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs36001065	0.80[EUR][1000 genomes]
rs3760298	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.95[TSI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3785628	0.85[JPT][hapmap]
rs3785631	0.92[CEU][hapmap];0.83[JPT][hapmap];0.91[TSI][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs3785633	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3815038	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3815039	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.93[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3826360	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4239134	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4435297	0.84[JPT][hapmap]
rs4791660	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4791661	0.83[EUR][1000 genomes]
rs4791662	0.92[CEU][hapmap];0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4792711	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4792717	0.85[JPT][hapmap]
rs4792719	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4792721	0.80[TSI][hapmap]
rs55676330	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62073587	0.81[EUR][1000 genomes]
rs6502482	0.85[JPT][hapmap];0.81[EUR][1000 genomes]
rs6502488	0.85[JPT][hapmap]
rs7207889	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7214695	0.85[JPT][hapmap]
rs7214891	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7217614	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7223346	0.85[JPT][hapmap]
rs72833498	0.88[EUR][1000 genomes]
rs758853	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.95[TSI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8070859	0.80[EUR][1000 genomes]
rs8076669	0.83[EUR][1000 genomes]
rs8076864	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];0.92[JPT][hapmap];0.86[MEX][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8079969	0.85[JPT][hapmap]
rs8080706	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9652828	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9889745	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9889822	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9890012	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.91[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9891379	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.93[TSI][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9898313	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9899002	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9902141	0.92[CEU][hapmap];0.82[MEX][hapmap];0.89[TSI][hapmap]
rs9903464	0.85[CEU][hapmap];0.82[MEX][hapmap];0.87[TSI][hapmap]
rs9905429	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9908031	0.92[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.83[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.91[TSI][hapmap];0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9909615	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9909697	0.92[CEU][hapmap]

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	nsv1062951	chr17:15561070-15890644	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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

mRNA abundance (count:22)

SNP	Gene	Cis/trans	Tissue	Source
rs10491104	TTC19	Cis_1M	lymphoblastoid	RTeQTL
rs10491104	LOC125150	cis	normal skin	skin_eQTL
rs10491104	CENPV	cis	Artery Tibial	GTEx
rs10491104	ADORA2B	cis	Adipose Subcutaneous	GTEx
rs10491104	ADORA2B	cis	Thyroid	GTEx
rs10491104	TTC19	cis	multi-tissue	Pritchard
rs10491104	ADORA2B	cis	lung	GTEx
rs10491104	NCOR1	cis	parietal	SCAN
rs10491104	LOC125150	cis	lesional skin	skin_eQTL
rs10491104	CENPV	cis	parietal	SCAN
rs10491104	PIGL	cis	multi-tissue	Pritchard
rs10491104	Hs.379903	cis	multi-tissue	Pritchard
rs10491104	ADORA2B	cis	Artery Tibial	GTEx
rs10491104	ADORA2B	cis	Muscle Skeletal	GTEx
rs10491104	TTC19	cis	lymphoblastoid	seeQTL
rs10491104	ZSWIM7	cis	Muscle Skeletal	GTEx
rs10491104	ZSWIM7	Cis_1M	lymphoblastoid	RTeQTL
rs10491104	ADORA2B	cis	multi-tissue	Pritchard
rs10491104	NCOR1	Cis_1M	lymphoblastoid	RTeQTL
rs10491104	LOC125150	cis	uninvolved skin	skin_eQTL
rs10491104	ADORA2B	cis	Nerve Tibial	GTEx
rs10491104	ADORA2B	cis	Esophagus Muscularis	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15870400-15902400	Weak transcription	Small Intestine	intestine
2	chr17:15870800-15902400	Weak transcription	Esophagus	oesophagus
3	chr17:15873200-15902200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr17:15874800-15902400	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr17:15876600-15885400	Weak transcription	Hela-S3	cervix
6	chr17:15877600-15888800	Weak transcription	NHDF-Ad	bronchial
7	chr17:15877800-15891200	Strong transcription	Fetal Muscle Leg	muscle
8	chr17:15878200-15901800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
9	chr17:15879000-15884600	Weak transcription	NH-A	brain
10	chr17:15879600-15891600	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr17:15880200-15901600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
12	chr17:15881200-15892800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr17:15881400-15901800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr17:15881600-15885400	Weak transcription	Primary neutrophils fromperipheralblood	blood
15	chr17:15881800-15888000	Weak transcription	HepG2	liver
16	chr17:15882200-15884800	Weak transcription	Lung	lung
17	chr17:15882200-15885400	Weak transcription	HSMMtube	muscle
18	chr17:15882200-15887600	Weak transcription	Aorta	Aorta
19	chr17:15883200-15884600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr17:15883200-15884600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr17:15883200-15885000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
22	chr17:15883200-15885400	Strong transcription	Fetal Brain Female	brain
23	chr17:15883200-15891200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr17:15883200-15894000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr17:15883400-15884600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr17:15883400-15886200	Strong transcription	Brain Germinal Matrix	brain
27	chr17:15883400-15894400	Strong transcription	Fetal Stomach	stomach
28	chr17:15883400-15896600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
29	chr17:15883600-15884600	Genic enhancers	Primary monocytes fromperipheralblood	blood
30	chr17:15883600-15884600	Strong transcription	Primary T helper cells PMA-I stimulated	--
31	chr17:15883600-15884600	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr17:15883600-15884600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr17:15883600-15884600	Strong transcription	Fetal Kidney	kidney
34	chr17:15883600-15884600	Genic enhancers	Rectal Mucosa Donor 29	rectum
35	chr17:15883600-15884600	Strong transcription	Rectal Smooth Muscle	rectum
36	chr17:15883600-15884800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr17:15883600-15884800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr17:15883600-15884800	Strong transcription	Cortex derived primary cultured neurospheres	brain
39	chr17:15883600-15884800	Genic enhancers	K562	blood
40	chr17:15883600-15885000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr17:15883600-15885000	Strong transcription	Muscle Satellite Cultured Cells	--
42	chr17:15883600-15885000	Strong transcription	A549	lung
43	chr17:15883600-15885400	Strong transcription	HSMM	muscle
44	chr17:15883600-15885600	Strong transcription	Brain Angular Gyrus	brain
45	chr17:15883600-15885600	Strong transcription	Right Ventricle	heart
46	chr17:15883600-15885600	Strong transcription	Spleen	Spleen
47	chr17:15883600-15885800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
48	chr17:15883600-15885800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr17:15883600-15885800	Strong transcription	Fetal Heart	heart
50	chr17:15883600-15886000	Strong transcription	Brain Anterior Caudate	brain

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