Variant report

Variant	rs2359612
Chromosome Location	chr16:31103796-31103797
allele	A/G
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	STAT3	chr16:31103764-31103967	MCF10A-Er-Src	breast:	n/a	chr16:31103866-31103877
2	POLR2A	chr16:31103479-31104145	U87	brain:	n/a	n/a
3	POLR2A	chr16:31103667-31119079	K562	blood:	n/a	n/a
4	MXI1	chr16:31103661-31104083	IMR90	lung:	n/a	n/a
5	STAT3	chr16:31103693-31104030	MCF10A-Er-Src	breast:	n/a	chr16:31103866-31103877
6	STAT3	chr16:31103767-31103967	MCF10A-Er-Src	breast:	n/a	chr16:31103866-31103877
7	POLR2A	chr16:31103479-31105091	U87	brain:	n/a	n/a
8	FOS	chr16:31103734-31103869	MCF10A-Er-Src	breast:	n/a	chr16:31103778-31103789 chr16:31103844-31103855 chr16:31103843-31103851 chr16:31103842-31103852 chr16:31103842-31103852

No.	Distal block	Cell Line	Cell type
1	chr16:31043165..31047105-chr16:31102487..31107326,5	MCF-7	breast:
2	chr16:31103018..31109714-chr16:31190079..31193155,12	K562	blood:
3	chr16:31012820..31015317-chr16:31101271..31104026,2	MCF-7	breast:
4	chr16:30968024..30972662-chr16:31101043..31106214,4	MCF-7	breast:
5	chr16:30958416..30960902-chr16:31103309..31106232,3	MCF-7	breast:
6	chr16:31098290..31102055-chr16:31103024..31106957,5	MCF-7	breast:
7	chr16:31102640..31104934-chr16:31119820..31121678,2	K562	blood:
8	chr16:31103434..31106492-chr16:31118402..31121759,4	K562	blood:
9	chr16:31008048..31010924-chr16:31103164..31107386,3	MCF-7	breast:
10	chr16:31102092..31103911-chr16:31104760..31107226,2	MCF-7	breast:
11	chr16:31103018..31108579-chr16:31189579..31192896,9	K562	blood:

Variant related genes	Relation type
PRSS53	TF binding region
ENSG00000103496	Chromatin interaction
ENSG00000151006	Chromatin interaction
ENSG00000252809	Chromatin interaction
ENSG00000167397	Chromatin interaction
ENSG00000089280	Chromatin interaction
ENSG00000099381	Chromatin interaction
ENSG00000175938	Chromatin interaction
ENSG00000103507	Chromatin interaction
ENSG00000255439	Chromatin interaction
ENSG00000261487	Chromatin interaction
ENSG00000099365	Chromatin interaction

Extended variants
information (count: 142 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:129)

rs_ID	r²[population]
rs1046276	1.00[JPT][hapmap]
rs1060506	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10782001	0.89[JPT][hapmap]
rs10782002	0.89[JPT][hapmap]
rs10871454	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11076	0.88[JPT][hapmap]
rs1108431	0.89[ASN][1000 genomes]
rs11150600	0.89[JPT][hapmap]
rs11150601	0.89[JPT][hapmap]
rs11150604	1.00[CEU][hapmap];1.00[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11640534	0.89[JPT][hapmap]
rs11640767	0.86[ASN][1000 genomes]
rs11640957	0.86[ASN][1000 genomes]
rs11640961	0.87[CEU][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.88[TSI][hapmap]
rs11642003	0.82[ASN][1000 genomes]
rs11642192	0.98[ASN][1000 genomes]
rs11647284	1.00[ASN][1000 genomes]
rs11647442	0.95[ASN][1000 genomes]
rs11649653	0.81[GIH][hapmap];1.00[JPT][hapmap]
rs11862744	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs11864806	1.00[ASN][1000 genomes]
rs11864839	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11865038	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11865499	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12102776	0.82[CHB][hapmap];0.92[CHD][hapmap]
rs12445650	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs12448321	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12597511	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.83[TSI][hapmap];0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12716981	0.95[ASN][1000 genomes]
rs12716982	0.95[ASN][1000 genomes]
rs12924903	1.00[JPT][hapmap]
rs12928852	0.89[JPT][hapmap]
rs12931046	0.89[JPT][hapmap]
rs12934418	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13708	0.89[JPT][hapmap]
rs14235	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1458201	0.89[JPT][hapmap]
rs1458202	0.89[JPT][hapmap]
rs1549293	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17839567	0.89[ASN][1000 genomes]
rs17839568	1.00[ASN][1000 genomes]
rs1870293	0.89[JPT][hapmap]
rs1978485	0.95[ASN][1000 genomes]
rs1978487	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.95[ASN][1000 genomes]
rs2032915	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.87[TSI][hapmap];0.83[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2054213	0.89[JPT][hapmap]
rs2288004	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2303222	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.88[MEX][hapmap];0.91[TSI][hapmap];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303223	1.00[CEU][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2305880	0.89[JPT][hapmap]
rs2305884	0.89[JPT][hapmap]
rs2855475	0.87[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.85[TSI][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28725459	0.91[ASN][1000 genomes]
rs28814987	1.00[ASN][1000 genomes]
rs2884738	0.95[ASN][1000 genomes]
rs34649473	0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs34898535	0.88[EUR][1000 genomes]
rs35351013	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35468353	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs35675346	1.00[JPT][hapmap]
rs35713203	1.00[ASN][1000 genomes]
rs3751855	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4468641	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4527034	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.89[MKK][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4889525	0.89[JPT][hapmap]
rs4889530	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4889599	0.89[JPT][hapmap]
rs4889603	0.84[CEU][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.83[MEX][hapmap];0.80[TSI][hapmap]
rs4889604	0.89[JPT][hapmap]
rs4889606	0.96[CEU][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.96[MEX][hapmap];0.95[TSI][hapmap]
rs4889609	1.00[JPT][hapmap]
rs4889619	0.84[ASN][1000 genomes]
rs4889620	0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4889623	0.82[CHB][hapmap]
rs55766044	0.95[ASN][1000 genomes]
rs55979739	0.89[ASN][1000 genomes]
rs56284083	0.89[ASN][1000 genomes]
rs56314408	0.95[ASN][1000 genomes]
rs56813533	0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57434408	0.91[ASN][1000 genomes]
rs58726213	0.87[ASN][1000 genomes]
rs59061704	0.86[ASN][1000 genomes]
rs59735493	0.95[ASN][1000 genomes]
rs60996860	0.91[ASN][1000 genomes]
rs61162043	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61320757	0.95[ASN][1000 genomes]
rs6565217	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6950	0.89[JPT][hapmap]
rs7187995	0.93[ASN][1000 genomes]
rs7190802	0.82[CHB][hapmap]
rs7196161	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7196726	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7197717	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7199949	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs7200879	1.00[JPT][hapmap]
rs7203999	0.82[CHD][hapmap];0.89[JPT][hapmap]
rs7204459	0.89[JPT][hapmap]
rs7206511	0.89[JPT][hapmap]
rs7294	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs729482	1.00[JPT][hapmap]
rs732172	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs732173	0.89[ASN][1000 genomes]
rs73530203	0.98[ASN][1000 genomes]
rs749670	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs749671	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[TSI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs749767	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.95[ASN][1000 genomes]
rs7500176	0.89[ASN][1000 genomes]
rs750952	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs8046707	0.84[GIH][hapmap];0.89[JPT][hapmap]
rs8047803	1.00[ASN][1000 genomes]
rs8050588	0.89[JPT][hapmap]
rs8050894	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8056842	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs8060857	0.89[JPT][hapmap]
rs8061047	0.93[ASN][1000 genomes]
rs8062719	0.89[JPT][hapmap]
rs881929	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs889548	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs889555	1.00[CHB][hapmap];0.92[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs897986	0.89[JPT][hapmap]
rs9923231	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9925964	1.00[CEU][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9926533	0.96[CEU][hapmap];0.82[CHD][hapmap];0.84[GIH][hapmap];0.89[JPT][hapmap];0.96[MEX][hapmap];0.91[TSI][hapmap]
rs9929899	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9934438	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9936329	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.87[TSI][hapmap];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9939417	1.00[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9939558	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9972727	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062456	chr16:30442166-31253997	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
2	nsv542898	chr16:30442166-31253997	Enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	437 gene(s)	inside rSNPs	diseases
3	nsv905729	chr16:30642867-31247924	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	387 gene(s)	inside rSNPs	diseases
4	nsv431451	chr16:30682399-31340999	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	350 gene(s)	inside rSNPs	diseases
5	nsv905734	chr16:30877544-31191482	Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
6	nsv905735	chr16:30890538-31247924	Strong transcription Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	264 gene(s)	inside rSNPs	diseases
7	nsv457483	chr16:30903679-31191482	Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription Enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
8	nsv571820	chr16:30903679-31191482	Enhancers Genic enhancers Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	253 gene(s)	inside rSNPs	diseases
9	esv1797877	chr16:30948643-31188432	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
10	nsv833193	chr16:30960796-31133604	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	109 gene(s)	inside rSNPs	diseases
11	nsv905740	chr16:31066249-31232437	Flanking Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
12	nsv905741	chr16:31066249-31247924	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	202 gene(s)	inside rSNPs	diseases
13	nsv905742	chr16:31102321-31247924	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	188 gene(s)	inside rSNPs	diseases

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs2359612	RP11-196G11.2	cis	Muscle Skeletal	GTEx
rs2359612	KAT8	cis	Skin Sun Exposed Lower leg	GTEx
rs2359612	STX1B	cis	cerebellum	SCAN
rs2359612	MYST1	cis	parietal	SCAN
rs2359612	ITGAX	cis	cerebellum	SCAN
rs2359612	ZNF668	cis	cerebellum	SCAN
rs2359612	HSD3B7	cis	Whole Blood	GTEx
rs2359612	MYST1	cis	lymphoblastoid	seeQTL
rs2359612	YPEL3	cis	cerebellum	SCAN
rs2359612	MYST1	cis	cerebellum	SCAN
rs2359612	KAT8	cis	Artery Tibial	GTEx
rs2359612	NCRNA00095	cis	cerebellum	SCAN

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31086400-31104400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr16:31086600-31104200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr16:31086600-31105200	Weak transcription	Right Atrium	heart
4	chr16:31087200-31103800	Strong transcription	NHLF	lung
5	chr16:31087200-31104200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr16:31087400-31104400	Strong transcription	Primary T cells from cord blood	blood
7	chr16:31087400-31104400	Strong transcription	Fetal Intestine Small	intestine
8	chr16:31087800-31104000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr16:31090000-31105200	Weak transcription	Fetal Kidney	kidney
10	chr16:31090400-31104200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr16:31091000-31104000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
12	chr16:31092000-31104600	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr16:31093000-31104600	Weak transcription	Small Intestine	intestine
14	chr16:31093400-31103800	Weak transcription	Fetal Brain Male	brain
15	chr16:31093600-31104400	Strong transcription	Cortex derived primary cultured neurospheres	brain
16	chr16:31093600-31104400	Strong transcription	Fetal Stomach	stomach
17	chr16:31093600-31104800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr16:31093800-31104200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
19	chr16:31093800-31104200	Weak transcription	Psoas Muscle	Psoas
20	chr16:31093800-31104600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr16:31094200-31104400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr16:31094600-31103800	Strong transcription	Brain Germinal Matrix	brain
23	chr16:31095400-31103800	Weak transcription	K562	blood
24	chr16:31098800-31104000	Strong transcription	GM12878-XiMat	blood
25	chr16:31099400-31103800	Strong transcription	HepG2	liver
26	chr16:31099600-31104000	Strong transcription	Dnd41	blood
27	chr16:31099800-31103800	Strong transcription	Skeletal Muscle Male	skeletal muscle
28	chr16:31100600-31103800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr16:31100800-31104000	Strong transcription	Fetal Muscle Leg	muscle
30	chr16:31100800-31104200	Strong transcription	Fetal Muscle Trunk	muscle
31	chr16:31100800-31104600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr16:31101600-31104200	Strong transcription	Left Ventricle	heart
33	chr16:31102400-31104000	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr16:31102400-31104400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr16:31102600-31104000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr16:31102600-31104000	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr16:31102600-31104000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr16:31102600-31104200	Weak transcription	Right Ventricle	heart
39	chr16:31102600-31104600	Weak transcription	Primary hematopoietic stem cells	blood
40	chr16:31102600-31104600	Weak transcription	HSMMtube	muscle
41	chr16:31102800-31103800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr16:31102800-31103800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr16:31102800-31103800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr16:31102800-31103800	Weak transcription	Esophagus	oesophagus
45	chr16:31102800-31103800	Weak transcription	Gastric	stomach
46	chr16:31102800-31103800	Weak transcription	Pancreas	Pancrea
47	chr16:31102800-31103800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr16:31102800-31103800	Weak transcription	HSMM	muscle
49	chr16:31102800-31103800	Weak transcription	Osteobl	bone
50	chr16:31102800-31104000	Weak transcription	Primary T cells fromperipheralblood	blood

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