Variant report

Variant	rs6050477
Chromosome Location	chr20:25221547-25221548
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr20:25180225..25182029-chr20:25219353..25221557,2	MCF-7	breast:
2	chr20:25212487..25223003-chr20:25225155..25231821,24	MCF-7	breast:
3	chr20:25210927..25216331-chr20:25216727..25222043,13	MCF-7	breast:
4	chr20:25219110..25221790-chr20:25233245..25235251,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000100994	Chromatin interaction

Extended variants
information (count: 148 )
Associated
traits (count: 19 )

rSNPs within LD-proxies of this variant (count:131)

rs_ID	r²[population]
rs1007707	0.81[CHD][hapmap];0.86[JPT][hapmap]
rs1044573	0.81[CEU][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs1046073	0.85[CEU][hapmap]
rs11100	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs1118963	0.84[ASN][1000 genomes]
rs1130694	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs13038092	1.00[CHD][hapmap];0.86[JPT][hapmap];0.91[ASN][1000 genomes]
rs1555330	0.84[ASN][1000 genomes]
rs1888997	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs1888999	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2151144	0.86[JPT][hapmap]
rs2227890	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2227892	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs2257233	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2257461	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2257705	0.85[CEU][hapmap];0.81[CHD][hapmap];0.86[JPT][hapmap]
rs2257712	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs2257991	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2258066	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2258135	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2258201	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs2258617	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2258719	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2258728	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2258769	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs2259837	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2260997	0.82[CEU][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap]
rs2261109	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs2261747	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2261784	0.92[CEU][hapmap];0.86[JPT][hapmap]
rs2268879	0.86[JPT][hapmap]
rs2297496	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2297497	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2387881	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2424698	0.86[JPT][hapmap]
rs2424699	0.86[JPT][hapmap]
rs2424704	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2474766	0.84[ASN][1000 genomes]
rs2474769	0.84[ASN][1000 genomes]
rs2474777	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs2482911	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2482918	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2482923	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2482927	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs2482931	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2482943	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs2500399	0.92[CEU][hapmap];0.85[JPT][hapmap]
rs2500405	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2500406	0.81[CHD][hapmap];0.86[JPT][hapmap]
rs2500424	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs2500432	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2500433	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs2500436	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs2500446	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs3746337	1.00[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs3761117	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs3787079	0.91[ASN][1000 genomes]
rs4619688	0.84[ASN][1000 genomes]
rs4813562	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs4815398	0.82[CEU][hapmap]
rs4815411	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs4815412	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs4815417	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs60043588	0.91[ASN][1000 genomes]
rs6037095	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6037097	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6037103	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6037105	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6050425	0.86[JPT][hapmap]
rs6050427	0.81[CHD][hapmap];0.86[JPT][hapmap]
rs6050431	0.81[CHD][hapmap]
rs6050463	0.84[ASN][1000 genomes]
rs6050472	0.92[AFR][1000 genomes];0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6050481	0.89[CEU][hapmap];0.84[ASN][1000 genomes]
rs6050513	1.00[CHD][hapmap];0.86[JPT][hapmap]
rs6050532	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs6050544	0.85[CEU][hapmap]
rs6050559	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6050561	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6050565	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6050567	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6050573	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6050590	0.86[JPT][hapmap]
rs6050598	0.89[CEU][hapmap];0.86[JPT][hapmap]
rs6050599	0.92[CEU][hapmap];0.86[JPT][hapmap]
rs6050611	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6076336	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6076347	0.82[CEU][hapmap];0.88[GIH][hapmap]
rs6083776	0.81[CHD][hapmap]
rs6083804	0.85[CEU][hapmap];0.86[JPT][hapmap]
rs6083805	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6083809	0.89[CEU][hapmap];0.86[JPT][hapmap]
rs6083818	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6083828	0.89[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6083853	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6083862	0.89[CEU][hapmap]
rs6107015	0.92[CEU][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap]
rs6107017	0.84[ASN][1000 genomes]
rs6107019	0.84[ASN][1000 genomes]
rs6107031	0.88[CEU][hapmap];0.86[JPT][hapmap]
rs6115093	0.81[CEU][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs6115094	0.84[ASN][1000 genomes]
rs6115100	0.84[ASN][1000 genomes]
rs6115101	0.89[CEU][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs6115109	0.84[ASN][1000 genomes]
rs6115140	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs6115159	0.88[CEU][hapmap];0.86[JPT][hapmap]
rs61272267	0.91[ASN][1000 genomes]
rs6132819	0.89[CEU][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs6132820	0.84[ASN][1000 genomes]
rs6132821	0.84[ASN][1000 genomes]
rs6132824	0.84[ASN][1000 genomes]
rs6138546	0.84[ASN][1000 genomes]
rs6138550	0.84[ASN][1000 genomes]
rs6138553	0.92[CEU][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs6138555	0.84[ASN][1000 genomes]
rs6138556	0.86[JPT][hapmap]
rs66650433	0.91[ASN][1000 genomes]
rs67049380	0.91[ASN][1000 genomes]
rs67352161	0.91[ASN][1000 genomes]
rs67864609	0.91[ASN][1000 genomes]
rs7020	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs7267979	0.85[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap]
rs7269584	0.91[ASN][1000 genomes]
rs7274130	0.85[ASN][1000 genomes]
rs73612661	0.91[ASN][1000 genomes]
rs7453	0.85[CEU][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs8115257	0.81[CEU][hapmap];0.89[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs8124539	1.00[CHD][hapmap];0.86[JPT][hapmap]
rs8184820	0.85[CEU][hapmap];1.00[CHD][hapmap];0.86[JPT][hapmap];0.84[ASN][1000 genomes]
rs9927	0.89[CHD][hapmap];0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062140	chr20:24807962-25304054	Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv544219	chr20:24807962-25304054	Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh 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	nsv1055341	chr20:24848416-25302271	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	nsv1066667	chr20:25133066-25238976	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
17	nsv544222	chr20:25133066-25238976	Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:19)

SNP	Gene	Cis/trans	Tissue	Source
rs6050477	PYGB	cis	cerebellum	SCAN
rs6050477	ABHD12	cis	Frontal Cortex	GTEx
rs6050477	ABHD12	cis	Brain Pons	GTEx
rs6050477	ABHD12	cis	lymphoblastoid	seeQTL
rs6050477	ABHD12	cis	uninvolved skin	skin_eQTL
rs6050477	PYGB	cis	multi-tissue	Pritchard
rs6050477	ABHD12	cis	Cerebellum	GTEx
rs6050477	GINS1	Cis_1M	lymphoblastoid	RTeQTL
rs6050477	HDHD4	cis	multi-tissue	Pritchard
rs6050477	NINL	cis	parietal	SCAN
rs6050477	GZF1	cis	cerebellum	SCAN
rs6050477	ABHD12	cis	Temporal Cortex	GTEx
rs6050477	ABHD12	cis	multi-tissue	Pritchard
rs6050477	ABHD12	Cis_1M	lymphoblastoid	RTeQTL
rs6050477	ABHD12	cis	lesional skin	skin_eQTL
rs6050477	DCLRE1C	trans	multi-tissue	Pritchard
rs6050477	NINL	cis	cerebellum	SCAN
rs6050477	PYGB	cis	Whole Blood	GTEx
rs6050477	C20orf22	cis	multi-tissue	Pritchard

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25204200-25222800	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr20:25213200-25221800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr20:25213400-25222200	Enhancers	HMEC	breast
4	chr20:25213600-25222200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr20:25214400-25223000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr20:25215200-25221800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr20:25215400-25223200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr20:25215600-25221600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr20:25215800-25221600	Weak transcription	Fetal Kidney	kidney
10	chr20:25215800-25222800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr20:25216000-25222800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr20:25217600-25227600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr20:25218800-25221600	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr20:25219000-25222000	Enhancers	HSMM	muscle
15	chr20:25219000-25226000	Weak transcription	Colonic Mucosa	Colon
16	chr20:25219000-25227400	Weak transcription	Colon Smooth Muscle	Colon
17	chr20:25219200-25221800	Enhancers	Muscle Satellite Cultured Cells	--
18	chr20:25219400-25221600	Weak transcription	Fetal Heart	heart
19	chr20:25219400-25221800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr20:25219400-25222000	Enhancers	NHEK	skin
21	chr20:25219400-25226800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr20:25219400-25226800	Weak transcription	Right Ventricle	heart
23	chr20:25219400-25227600	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr20:25219400-25228000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr20:25219600-25222800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr20:25219600-25227000	Weak transcription	NHDF-Ad	bronchial
27	chr20:25219800-25221600	Weak transcription	HSMMtube	muscle
28	chr20:25219800-25227400	Weak transcription	NHLF	lung
29	chr20:25220000-25221600	Weak transcription	Osteobl	bone
30	chr20:25220200-25221600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
31	chr20:25220200-25222200	Enhancers	A549	lung
32	chr20:25220200-25227000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr20:25220400-25221600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr20:25220400-25227400	Weak transcription	Esophagus	oesophagus
35	chr20:25220600-25226800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr20:25220600-25227200	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr20:25220800-25221600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr20:25220800-25221600	Weak transcription	K562	blood
39	chr20:25220800-25221800	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr20:25220800-25221800	Weak transcription	NH-A	brain
41	chr20:25220800-25226000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
42	chr20:25221000-25222200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr20:25221200-25222000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr20:25221400-25221800	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr20:25221400-25221800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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