Variant report

Variant	rs11862744
Chromosome Location	chr16:31057800-31057801
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	chr16:31050910..31053194-chr16:31055951..31058904,2	MCF-7	breast:
2	chr16:31054525..31057827-chr16:31082936..31085986,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000167395	Chromatin interaction
ENSG00000167394	Chromatin interaction

Extended variants
information (count: 153 )
Associated
traits (count: 22 )

rSNPs within LD-proxies of this variant (count:141)

rs_ID	r²[population]
rs1046276	0.88[GIH][hapmap];1.00[JPT][hapmap]
rs1060506	1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.84[ASN][1000 genomes]
rs10782001	0.89[JPT][hapmap]
rs10782002	0.88[GIH][hapmap];0.89[JPT][hapmap];0.83[TSI][hapmap]
rs10871454	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11076	0.88[JPT][hapmap]
rs1108431	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11150599	0.88[JPT][hapmap]
rs11150600	0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs11150601	0.91[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs11150604	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11640534	0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs11640767	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11640957	0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11640961	0.89[JPT][hapmap]
rs11642192	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11647284	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11647442	0.84[ASN][1000 genomes]
rs11649653	1.00[JPT][hapmap]
rs11864806	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11864839	1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11865038	0.93[ASW][hapmap];0.92[CEU][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.94[MKK][hapmap];0.83[YRI][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11865499	1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.84[ASN][1000 genomes]
rs12102776	0.92[CHD][hapmap]
rs12445568	0.91[CEU][hapmap];1.00[CHB][hapmap];0.88[GIH][hapmap];0.95[MEX][hapmap];0.92[TSI][hapmap]
rs12445650	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12447930	0.80[EUR][1000 genomes]
rs12448321	1.00[ASN][1000 genomes]
rs12597511	1.00[CHD][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs12716981	0.84[ASN][1000 genomes]
rs12716982	0.84[ASN][1000 genomes]
rs12924903	0.88[GIH][hapmap];1.00[JPT][hapmap]
rs12926295	0.88[JPT][hapmap]
rs12928852	0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs12930545	0.88[GIH][hapmap];0.85[TSI][hapmap]
rs12931046	0.87[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.80[TSI][hapmap]
rs12934418	1.00[ASN][1000 genomes]
rs13708	0.91[CEU][hapmap];0.89[JPT][hapmap]
rs14235	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs1458201	0.89[JPT][hapmap]
rs1458202	0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs1549293	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs17839567	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17839568	0.91[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1870293	0.91[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.80[TSI][hapmap]
rs1978485	0.84[ASN][1000 genomes]
rs1978487	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2032915	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs2054213	0.91[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs2288004	1.00[ASN][1000 genomes]
rs2303222	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2303223	1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs2305880	0.91[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.87[TSI][hapmap]
rs2305884	0.91[CEU][hapmap];0.85[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs2359612	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs2855475	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs28725459	0.81[ASN][1000 genomes]
rs28814987	0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2884738	0.84[ASN][1000 genomes]
rs34649473	0.83[ASN][1000 genomes]
rs34898535	0.87[ASN][1000 genomes]
rs35351013	0.82[ASN][1000 genomes]
rs35468353	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35675346	1.00[JPT][hapmap]
rs35713203	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs35961830	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3751855	0.91[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3813020	0.88[GIH][hapmap];0.82[TSI][hapmap]
rs4468641	0.92[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.91[MKK][hapmap];0.88[TSI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4527034	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs4889525	0.87[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs4889526	0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889530	0.89[ASN][1000 genomes]
rs4889599	0.91[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs4889603	0.89[JPT][hapmap]
rs4889604	0.87[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.80[TSI][hapmap]
rs4889606	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs4889609	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];0.97[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4889620	0.84[ASN][1000 genomes]
rs4889651	0.88[JPT][hapmap]
rs4889653	0.88[JPT][hapmap]
rs55766044	0.84[ASN][1000 genomes]
rs55979739	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56284083	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56314408	0.84[ASN][1000 genomes]
rs56813533	0.82[ASN][1000 genomes]
rs57434408	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs57576577	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58726213	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59061704	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs59735493	0.84[ASN][1000 genomes]
rs60996860	0.81[ASN][1000 genomes]
rs61162043	0.89[ASN][1000 genomes]
rs61320757	0.84[ASN][1000 genomes]
rs6565217	0.87[ASW][hapmap];0.92[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[MEX][hapmap];0.91[MKK][hapmap];0.83[TSI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6950	0.91[CEU][hapmap];0.89[JPT][hapmap]
rs7184567	1.00[CEU][hapmap];0.92[YRI][hapmap]
rs7187995	0.82[ASN][1000 genomes]
rs7196161	0.89[ASN][1000 genomes]
rs7196726	0.92[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7197717	0.93[ASW][hapmap];0.92[CEU][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.91[MEX][hapmap];0.94[MKK][hapmap];0.88[TSI][hapmap];0.83[YRI][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7199949	0.91[CEU][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7200879	1.00[JPT][hapmap]
rs7203999	0.91[CEU][hapmap];1.00[CHB][hapmap];0.82[CHD][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];1.00[MEX][hapmap];0.97[TSI][hapmap]
rs7204459	0.87[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.80[TSI][hapmap]
rs7206511	0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs7294	0.92[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs729482	0.91[CEU][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.85[TSI][hapmap]
rs732172	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.90[TSI][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs732173	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73530203	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs749670	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs749671	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs749767	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7500176	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs750952	0.92[CEU][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.82[TSI][hapmap];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8046707	0.89[JPT][hapmap]
rs8047803	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8050588	0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs8050894	1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs8056842	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8060857	0.87[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap]
rs8061047	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8062719	0.91[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap]
rs8063565	0.88[JPT][hapmap]
rs881929	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs889548	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs889555	0.92[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs897986	0.91[CEU][hapmap];0.88[GIH][hapmap];0.89[JPT][hapmap];0.85[TSI][hapmap]
rs9673641	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9923231	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs9925964	0.84[ASN][1000 genomes]
rs9926533	1.00[CHB][hapmap];0.82[CHD][hapmap];0.89[JPT][hapmap]
rs9929899	0.98[ASN][1000 genomes]
rs9933843	0.88[JPT][hapmap]
rs9934438	1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs9936329	1.00[CHD][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs9938550	0.91[CEU][hapmap];0.88[GIH][hapmap];0.87[TSI][hapmap]
rs9939417	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9939558	1.00[ASN][1000 genomes]
rs9972727	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 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	nsv1064134	chr16:30640293-31087327	Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	238 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	nsv916994	chr16:30971725-31078117	Active TSS Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

mRNA abundance (count:22)

SNP	Gene	Cis/trans	Tissue	Source
rs11862744	ZNF48	cis	cerebellum	SCAN
rs11862744	HSD3B7	cis	Esophagus Mucosa	GTEx
rs11862744	TAOK2	cis	parietal	SCAN
rs11862744	RP11-196G11.2	cis	Esophagus Muscularis	GTEx
rs11862744	MYST1	cis	cerebellum	SCAN
rs11862744	ZNF747	cis	parietal	SCAN
rs11862744	KAT8	cis	Artery Tibial	GTEx
rs11862744	MYST1	cis	lymphoblastoid	seeQTL
rs11862744	STX4	Cis_1M	lymphoblastoid	RTeQTL
rs11862744	NCRNA00095	cis	cerebellum	SCAN
rs11862744	MYST1	Cis_1M	lymphoblastoid	RTeQTL
rs11862744	VKORC1	cis	cerebellum	SCAN
rs11862744	RP11-196G11.2	cis	lung	GTEx
rs11862744	KAT8	cis	Skin Sun Exposed Lower leg	GTEx
rs11862744	RABEP2	cis	cerebellum	SCAN
rs11862744	HSD3B7	cis	Muscle Skeletal	GTEx
rs11862744	STX1B	cis	Thyroid	GTEx
rs11862744	MYST1	cis	parietal	SCAN
rs11862744	STX4	cis	lymphoblastoid	seeQTL
rs11862744	YPEL3	cis	parietal	SCAN
rs11862744	ZNF785	cis	lymphoblastoid	seeQTL
rs11862744	RP11-196G11.2	cis	Muscle Skeletal	GTEx

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:31046000-31071000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr16:31046000-31083200	Weak transcription	Right Atrium	heart
3	chr16:31046200-31058200	Weak transcription	HUVEC	blood vessel
4	chr16:31046200-31063000	Weak transcription	Hela-S3	cervix
5	chr16:31046200-31063200	Weak transcription	HMEC	breast
6	chr16:31048200-31063200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr16:31048200-31063400	Weak transcription	K562	blood
8	chr16:31048200-31071400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr16:31048400-31061600	Weak transcription	NHDF-Ad	bronchial
10	chr16:31049600-31075600	Weak transcription	Psoas Muscle	Psoas
11	chr16:31051000-31063200	Weak transcription	NH-A	brain
12	chr16:31051200-31071000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr16:31051400-31083000	Weak transcription	Fetal Lung	lung
14	chr16:31052000-31071800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr16:31052000-31083400	Weak transcription	Primary B cells from cord blood	blood
16	chr16:31052400-31074400	Weak transcription	Primary hematopoietic stem cells	blood
17	chr16:31052600-31063600	Weak transcription	Small Intestine	intestine
18	chr16:31053800-31072000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr16:31054000-31063400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr16:31054000-31069200	Weak transcription	Fetal Brain Female	brain
21	chr16:31054000-31072600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
22	chr16:31054000-31083200	Weak transcription	Fetal Kidney	kidney
23	chr16:31054200-31057800	Enhancers	HepG2	liver
24	chr16:31054200-31071000	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr16:31054200-31076200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr16:31054400-31060800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr16:31054400-31071800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr16:31054400-31072000	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr16:31054600-31060800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr16:31054600-31061600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr16:31054600-31063200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr16:31054600-31063400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr16:31054600-31071600	Weak transcription	Dnd41	blood
34	chr16:31054600-31071800	Weak transcription	GM12878-XiMat	blood
35	chr16:31054600-31072000	Weak transcription	Esophagus	oesophagus
36	chr16:31054600-31072200	Weak transcription	Colonic Mucosa	Colon
37	chr16:31054800-31059800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr16:31054800-31060600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr16:31054800-31061400	Weak transcription	HSMM	muscle
40	chr16:31054800-31063200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr16:31054800-31063200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr16:31054800-31063200	Weak transcription	HSMMtube	muscle
43	chr16:31054800-31064600	Weak transcription	Sigmoid Colon	Sigmoid Colon
44	chr16:31054800-31068800	Weak transcription	Brain Inferior Temporal Lobe	brain
45	chr16:31054800-31069000	Weak transcription	Thymus	Thymus
46	chr16:31054800-31069200	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr16:31054800-31071000	Weak transcription	Fetal Thymus	thymus
48	chr16:31054800-31071400	Weak transcription	Brain Hippocampus Middle	brain
49	chr16:31054800-31071600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr16:31054800-31071600	Weak transcription	Gastric	stomach

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