Variant report

Variant	rs6083824
Chromosome Location	chr20:25363057-25363058
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr20:25360007..25361800-chr20:25361801..25365335,3	K562	blood:
2	chr20:25360394..25363180-chr20:25371562..25374296,2	MCF-7	breast:
3	chr20:25362177..25366846-chr20:25370134..25372781,8	MCF-7	breast:
4	chr20:25361123..25364649-chr20:25367842..25371667,4	K562	blood:
5	chr20:25356181..25358893-chr20:25361208..25363554,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000100997	Chromatin interaction

Extended variants
information (count: 167 )
Associated
traits (count: 16 )

rSNPs within LD-proxies of this variant (count:149)

rs_ID	r²[population]
rs1046073	0.82[CEU][hapmap]
rs1047171	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs11087521	0.85[CEU][hapmap]
rs11100	0.81[CEU][hapmap]
rs1130694	0.85[CEU][hapmap];0.89[GIH][hapmap]
rs12428	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs13040726	0.95[YRI][hapmap]
rs1541061	0.87[CEU][hapmap]
rs1888997	0.82[CEU][hapmap]
rs1888999	0.82[CEU][hapmap]
rs1983974	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.96[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2151144	0.81[CEU][hapmap]
rs2227890	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2227892	0.85[CEU][hapmap]
rs2257233	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2257461	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2257649	0.83[AFR][1000 genomes];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2257705	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2257712	0.85[CEU][hapmap]
rs2257991	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2258066	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs2258135	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2258201	0.82[CEU][hapmap]
rs2258617	0.82[CEU][hapmap];0.91[GIH][hapmap]
rs2258719	0.82[CEU][hapmap]
rs2258728	0.82[CEU][hapmap];0.91[GIH][hapmap]
rs2258769	0.82[CEU][hapmap]
rs2259837	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2259961	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2260997	0.93[GIH][hapmap]
rs2261109	0.82[CEU][hapmap]
rs2261747	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2261784	0.84[CEU][hapmap]
rs2297496	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2297497	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2387881	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs2424703	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2424704	0.82[CEU][hapmap];0.91[GIH][hapmap]
rs2474765	0.81[EUR][1000 genomes]
rs2474777	0.82[CEU][hapmap];0.95[GIH][hapmap]
rs2474780	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2482911	0.82[CEU][hapmap]
rs2482918	0.82[CEU][hapmap]
rs2482923	0.82[CEU][hapmap]
rs2482927	0.82[CEU][hapmap]
rs2482931	0.82[CEU][hapmap]
rs2482943	0.82[CEU][hapmap]
rs2500399	0.81[CEU][hapmap]
rs2500405	0.82[CEU][hapmap]
rs2500424	0.81[CEU][hapmap]
rs2500430	0.86[EUR][1000 genomes]
rs2500432	0.82[CEU][hapmap]
rs2500433	0.82[CEU][hapmap]
rs2500436	0.82[CEU][hapmap]
rs2500446	0.82[CEU][hapmap]
rs2856	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs2983489	0.81[EUR][1000 genomes]
rs35735333	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs374701	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs3761117	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs376742	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs390123	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs397119	0.82[CEU][hapmap];0.91[GIH][hapmap]
rs398036	0.82[CEU][hapmap];0.91[GIH][hapmap]
rs400357	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs404148	0.92[CEU][hapmap]
rs404775	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.93[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs405822	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[YRI][hapmap];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs409853	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[YRI][hapmap];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs417110	0.91[GIH][hapmap]
rs422148	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs422844	0.82[CEU][hapmap]
rs431579	0.91[GIH][hapmap]
rs433352	0.91[GIH][hapmap]
rs437635	0.81[CEU][hapmap]
rs4423675	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs443009	1.00[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.98[GIH][hapmap];0.93[LWK][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.95[YRI][hapmap];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs446649	0.91[GIH][hapmap]
rs449370	0.91[GIH][hapmap]
rs449801	0.89[CEU][hapmap]
rs454723	0.82[CEU][hapmap]
rs4813562	0.85[CEU][hapmap];0.93[GIH][hapmap];0.81[EUR][1000 genomes]
rs4815398	0.85[CEU][hapmap]
rs4815400	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4815409	0.81[EUR][1000 genomes]
rs4815411	0.85[CEU][hapmap];0.93[GIH][hapmap];0.81[EUR][1000 genomes]
rs4815412	0.85[CEU][hapmap];0.93[GIH][hapmap];0.81[EUR][1000 genomes]
rs4815413	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4815414	0.81[EUR][1000 genomes]
rs4815417	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs4815429	0.82[AMR][1000 genomes]
rs4815431	0.82[AMR][1000 genomes]
rs6037095	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs6037097	0.85[CEU][hapmap];0.93[GIH][hapmap];0.81[EUR][1000 genomes]
rs6037099	0.81[EUR][1000 genomes]
rs6037103	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs6037105	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs6050532	0.82[CEU][hapmap]
rs6050544	0.82[CEU][hapmap]
rs6050559	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs6050561	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs6050564	0.81[EUR][1000 genomes]
rs6050565	0.85[CEU][hapmap];0.93[GIH][hapmap];0.81[EUR][1000 genomes]
rs6050567	0.85[CEU][hapmap];0.93[GIH][hapmap];0.81[EUR][1000 genomes]
rs6050573	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs6050598	0.85[CEU][hapmap];0.95[GIH][hapmap]
rs6050599	0.84[CEU][hapmap]
rs6050611	0.82[CEU][hapmap]
rs6050617	0.85[CEU][hapmap]
rs6050626	0.84[CEU][hapmap];0.93[GIH][hapmap]
rs6050679	0.92[CEU][hapmap];1.00[CHB][hapmap];0.96[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.82[AMR][1000 genomes]
rs6076336	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs6076339	0.81[EUR][1000 genomes]
rs6076343	0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6076347	0.92[CEU][hapmap]
rs6076358	0.82[EUR][1000 genomes]
rs6083804	0.82[CEU][hapmap]
rs6083805	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs6083809	0.85[CEU][hapmap]
rs6083818	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs6083828	0.85[CEU][hapmap];0.93[GIH][hapmap]
rs6083845	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[YRI][hapmap];0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6083851	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6083853	0.82[CEU][hapmap]
rs6083860	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6083862	0.85[CEU][hapmap];0.84[GIH][hapmap]
rs6107015	0.81[CEU][hapmap]
rs6107027	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6107031	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs6107033	0.81[EUR][1000 genomes]
rs6107045	0.82[CEU][hapmap]
rs6107047	0.81[CEU][hapmap]
rs6115140	0.82[CEU][hapmap]
rs6115156	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6115159	0.84[CEU][hapmap];0.81[EUR][1000 genomes]
rs6115188	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6115191	0.82[CEU][hapmap]
rs6138553	0.81[CEU][hapmap]
rs6138572	0.82[CEU][hapmap]
rs6138575	0.82[CEU][hapmap]
rs6138593	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7020	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs7267979	0.82[CEU][hapmap];0.93[GIH][hapmap]
rs7270835	0.81[CEU][hapmap]
rs7453	0.91[GIH][hapmap]
rs761025	0.81[CEU][hapmap]
rs84816	0.91[GIH][hapmap]
rs869358	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9927	0.87[GIH][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	nsv1063494	chr20:25067286-25468557	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv1063016	chr20:25067286-25475629	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
3	nsv1065101	chr20:25068046-25466542	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS 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 target site	53 gene(s)	inside rSNPs	diseases
4	nsv544220	chr20:25068046-25466542	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
5	nsv531480	chr20:25070067-25472684	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
6	nsv585746	chr20:25071454-25470056	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
7	nsv1062742	chr20:25071454-25475629	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
8	nsv949389	chr20:25071454-25506582	Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
9	nsv531481	chr20:25080583-25448944	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
10	nsv949479	chr20:25096494-25467359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
11	nsv1061109	chr20:25101715-25472685	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
12	nsv544221	chr20:25101715-25472685	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
13	nsv833948	chr20:25231726-25410540	Strong transcription Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
14	nsv482647	chr20:25308912-25481982	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription 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	21 gene(s)	inside rSNPs	diseases
15	nsv1056997	chr20:25316663-25492339	Strong transcription Weak transcription Genic enhancers Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
16	nsv1061058	chr20:25327960-25388841	Flanking Active TSS Enhancers Strong transcription Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
17	nsv964440	chr20:25351740-25387631	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	13 gene(s)	inside rSNPs	diseases
18	nsv1067379	chr20:25355484-25593240	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases

mRNA abundance (count:16)

SNP	Gene	Cis/trans	Tissue	Source
rs6083824	PYGB	cis	cerebellum	SCAN
rs6083824	ABHD12	cis	multi-tissue	Pritchard
rs6083824	PYGB	cis	Whole Blood	GTEx
rs6083824	PYGB	cis	multi-tissue	Pritchard
rs6083824	ABHD12	cis	lymphoblastoid	seeQTL
rs6083824	ABHD12	cis	cerebellum	SCAN
rs6083824	NINL	cis	cerebellum	SCAN
rs6083824	GINS1	cis	parietal	SCAN
rs6083824	PYGB	cis	lymphoblastoid	seeQTL
rs6083824	ABHD12	cis	parietal	SCAN
rs6083824	NINL	cis	parietal	SCAN
rs6083824	ENTPD6	cis	cerebellum	SCAN
rs6083824	NINL	cis	Thyroid	GTEx
rs6083824	ZNF337	cis	cerebellum	SCAN
rs6083824	GINS1	Cis_1M	lymphoblastoid	RTeQTL
rs6083824	ABHD12	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25337000-25370000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr20:25338000-25369400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr20:25342200-25370000	Weak transcription	Primary hematopoietic stem cells	blood
4	chr20:25343800-25370000	Weak transcription	Small Intestine	intestine
5	chr20:25345200-25369800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr20:25345800-25363200	Weak transcription	Esophagus	oesophagus
7	chr20:25345800-25369800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr20:25345800-25370000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr20:25345800-25370000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr20:25351400-25369600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr20:25351800-25370000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr20:25353000-25370000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr20:25353800-25365200	Weak transcription	Fetal Lung	lung
14	chr20:25353800-25368800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr20:25353800-25370000	Weak transcription	Adipose Nuclei	Adipose
16	chr20:25353800-25370000	Weak transcription	HSMM	muscle
17	chr20:25354000-25363800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr20:25354000-25368800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr20:25354000-25369800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr20:25354000-25369800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr20:25354000-25369800	Weak transcription	NH-A	brain
22	chr20:25354000-25369800	Weak transcription	NHEK	skin
23	chr20:25354800-25370000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr20:25355800-25369800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr20:25357800-25369800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr20:25358000-25365000	Weak transcription	Ovary	ovary
27	chr20:25358000-25368800	Weak transcription	Osteobl	bone
28	chr20:25358000-25369800	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr20:25358000-25370000	Weak transcription	Fetal Muscle Leg	muscle
30	chr20:25358000-25370000	Weak transcription	Rectal Smooth Muscle	rectum
31	chr20:25358200-25369800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr20:25359000-25364200	Strong transcription	Dnd41	blood
33	chr20:25359200-25364800	Weak transcription	Fetal Brain Female	brain
34	chr20:25359200-25370000	Weak transcription	HSMMtube	muscle
35	chr20:25359400-25369800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr20:25359600-25363600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
37	chr20:25359600-25364000	Enhancers	Brain Hippocampus Middle	brain
38	chr20:25359600-25365400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr20:25359800-25363400	Weak transcription	Stomach Mucosa	stomach
40	chr20:25359800-25369600	Weak transcription	Primary T cells fromperipheralblood	blood
41	chr20:25360000-25365000	Weak transcription	Fetal Intestine Small	intestine
42	chr20:25360000-25369800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr20:25360000-25370000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
44	chr20:25360000-25370000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr20:25360000-25370000	Weak transcription	Duodenum Mucosa	Duodenum
46	chr20:25360200-25363200	Weak transcription	Fetal Intestine Large	intestine
47	chr20:25360200-25370000	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr20:25360400-25363600	Strong transcription	Fetal Stomach	stomach
49	chr20:25360400-25370000	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr20:25360600-25363600	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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