Variant report

Variant	rs73341122
Chromosome Location	chr20:25227374-25227375
allele	G/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	POLR2A	chr20:25227358-25229473	MCF-7	breast:	n/a	n/a
2	EBF1	chr20:25227105-25227459	GM12878	blood:	n/a	chr20:25227294-25227305
3	CEBPB	chr20:25227202-25227559	HepG2	liver:	n/a	chr20:25227370-25227381 chr20:25227249-25227260 chr20:25227249-25227260
4	POLR2A	chr20:25226914-25229518	A549	lung:	n/a	n/a
5	CEBPB	chr20:25226950-25227737	A549	lung:	n/a	chr20:25227370-25227381 chr20:25227249-25227260 chr20:25227249-25227260
6	ARID3A	chr20:25227258-25228233	HepG2	liver:	n/a	n/a
7	POLR2A	chr20:25226835-25229543	A549	lung:	n/a	n/a
8	CREB1	chr20:25227264-25229533	A549	lung:	n/a	n/a
9	POLR2A	chr20:25226530-25230405	PANC-1	pancreas:	n/a	n/a
10	POLR2A	chr20:25227236-25227785	K562	blood:	n/a	n/a
11	GATA3	chr20:25227225-25227573	SH-SY5Y	brain:	n/a	chr20:25227237-25227246
12	POLR2A	chr20:25227339-25227531	A549	lung:	n/a	n/a
13	MXI1	chr20:25227367-25230166	IMR90	lung:	n/a	n/a
14	CEBPB	chr20:25227254-25227523	K562	blood:	n/a	chr20:25227370-25227381
15	RUNX3	chr20:25227073-25227409	GM12878	blood:	n/a	n/a
16	CTCF	chr20:25227299-25230561	A549	lung:	n/a	chr20:25229433-25229446 chr20:25227553-25227566
17	POLR2A	chr20:25227206-25229511	Raji	blood:	n/a	n/a
18	POLR2A	chr20:25226929-25227558	PANC-1	pancreas:	n/a	n/a
19	GATA2	chr20:25227055-25227602	SH-SY5Y	brain:	n/a	chr20:25227237-25227246
20	EBF1	chr20:25227174-25227472	GM12878	blood:	n/a	chr20:25227294-25227305
21	EBF1	chr20:25227132-25227422	GM12878	blood:	n/a	chr20:25227294-25227305
22	TCF12	chr20:25227034-25229635	A549	lung:	n/a	chr20:25228350-25228360 chr20:25227192-25227199
23	MAZ	chr20:25227102-25230389	IMR90	lung:	n/a	chr20:25229402-25229412
24	RAD21	chr20:25227374-25228077	A549	lung:	n/a	n/a
25	CEBPB	chr20:25227196-25227565	A549	lung:	n/a	chr20:25227370-25227381 chr20:25227249-25227260 chr20:25227249-25227260
26	MXI1	chr20:25227089-25230580	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:25204037..25205721-chr20:25227160..25229400,2	K562	blood:
2	chr20:25208292..25210129-chr20:25227027..25228548,2	MCF-7	breast:
3	chr20:25226304..25227809-chr20:25275139..25278038,2	MCF-7	breast:
4	chr20:25057289..25058975-chr20:25226619..25228863,2	MCF-7	breast:
5	chr20:25204221..25206637-chr20:25227058..25229400,2	K562	blood:
6	chr20:25200007..25207026-chr20:25227086..25230373,11	MCF-7	breast:
7	chr20:25174902..25179249-chr20:25225017..25231959,9	MCF-7	breast:
8	chr20:25202506..25206898-chr20:25226343..25231297,7	MCF-7	breast:
9	chr20:25174010..25179528-chr20:25225802..25231331,13	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABHD12-1	chr20:25227084-25227480	XLOC_013706

Variant related genes	Relation type
PYGB	TF binding region
ENSG00000197586	Chromatin interaction
ENSG00000100987	Chromatin interaction

Extended variants
information (count: 116 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs12106059	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12106164	1.00[EUR][1000 genomes]
rs12373881	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2500428	1.00[EUR][1000 genomes]
rs28435893	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28439563	1.00[EUR][1000 genomes]
rs28551104	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35073849	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56273742	1.00[EUR][1000 genomes]
rs57218388	1.00[EUR][1000 genomes]
rs57293656	1.00[EUR][1000 genomes]
rs58189090	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58410604	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58593226	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58709664	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58722006	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58953621	1.00[AMR][1000 genomes]
rs58957358	1.00[EUR][1000 genomes]
rs59431257	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59857017	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60459445	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60479943	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6050367	1.00[EUR][1000 genomes]
rs60893899	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7270236	1.00[EUR][1000 genomes]
rs7270324	1.00[AMR][1000 genomes]
rs7274585	1.00[AMR][1000 genomes]
rs73331819	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73331822	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73331824	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73331833	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73331834	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73331856	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73331880	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73331881	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73333142	1.00[EUR][1000 genomes]
rs73333167	1.00[EUR][1000 genomes]
rs73333174	1.00[EUR][1000 genomes]
rs73333187	1.00[EUR][1000 genomes]
rs73333506	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73333515	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73333541	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73337199	1.00[EUR][1000 genomes]
rs73339096	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73339099	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73339100	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341103	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341112	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341114	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341120	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341124	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341128	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341131	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341135	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341140	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341143	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341155	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341157	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73341171	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73343010	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73343043	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73343050	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73343053	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73343058	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73343076	1.00[AMR][1000 genomes]
rs73343090	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73343097	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345003	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345011	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345016	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345021	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345030	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345040	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345068	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345069	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345071	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345073	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345082	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345087	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73345088	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73347016	1.00[AMR][1000 genomes]
rs73347023	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73347042	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73347058	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73347066	1.00[AMR][1000 genomes]
rs73906068	1.00[EUR][1000 genomes]
rs73906070	1.00[EUR][1000 genomes]
rs73906071	1.00[EUR][1000 genomes]
rs73906072	1.00[EUR][1000 genomes]
rs8114108	1.00[EUR][1000 genomes]
rs8115188	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8117413	1.00[AMR][1000 genomes]
rs8118017	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8119273	1.00[EUR][1000 genomes]
rs8120601	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8121557	1.00[EUR][1000 genomes]
rs8123929	1.00[EUR][1000 genomes]
rs8123947	1.00[AMR][1000 genomes]

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	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
18	nsv828708	chr20:25223895-25231601	Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25217600-25227600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr20:25219000-25227400	Weak transcription	Colon Smooth Muscle	Colon
3	chr20:25219400-25227600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr20:25219400-25228000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr20:25219800-25227400	Weak transcription	NHLF	lung
6	chr20:25220400-25227400	Weak transcription	Esophagus	oesophagus
7	chr20:25222000-25227400	Weak transcription	Fetal Kidney	kidney
8	chr20:25222000-25227400	Weak transcription	HSMMtube	muscle
9	chr20:25222000-25227600	Weak transcription	Fetal Lung	lung
10	chr20:25222400-25227400	Weak transcription	NH-A	brain
11	chr20:25223200-25227400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr20:25223400-25227400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr20:25223600-25227800	Weak transcription	Brain Germinal Matrix	brain
14	chr20:25223800-25227600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr20:25226000-25227400	Enhancers	Hela-S3	cervix
16	chr20:25226200-25227600	Enhancers	Fetal Intestine Large	intestine
17	chr20:25226200-25227600	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr20:25226200-25227600	Enhancers	GM12878-XiMat	blood
19	chr20:25226600-25227400	Weak transcription	HUVEC	blood vessel
20	chr20:25226600-25227600	Enhancers	Fetal Intestine Small	intestine
21	chr20:25226800-25227400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr20:25226800-25227400	Enhancers	Muscle Satellite Cultured Cells	--
23	chr20:25226800-25227400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr20:25226800-25227600	Enhancers	Right Ventricle	heart
25	chr20:25226800-25227800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr20:25226800-25227800	Flanking Active TSS	A549	lung
27	chr20:25226800-25228000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr20:25226800-25228000	Flanking Active TSS	HMEC	breast
29	chr20:25227000-25227400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr20:25227000-25227400	Enhancers	Dnd41	blood
31	chr20:25227000-25227400	Weak transcription	Monocytes-CD14+_RO01746	blood
32	chr20:25227000-25227400	Enhancers	Osteobl	bone
33	chr20:25227000-25227600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr20:25227000-25227600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
35	chr20:25227000-25227600	Enhancers	Breast Myoepithelial Primary Cells	Breast
36	chr20:25227000-25227600	Enhancers	Liver	Liver
37	chr20:25227000-25227600	Enhancers	Left Ventricle	heart
38	chr20:25227000-25227600	Enhancers	Pancreas	Pancrea
39	chr20:25227000-25227600	Enhancers	HSMM	muscle
40	chr20:25227000-25227600	Enhancers	K562	blood
41	chr20:25227000-25227600	Enhancers	NHDF-Ad	bronchial
42	chr20:25227000-25227800	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr20:25227000-25227800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
44	chr20:25227000-25227800	Enhancers	Thymus	Thymus
45	chr20:25227000-25228000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr20:25227000-25228000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr20:25227000-25228000	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
48	chr20:25227000-25228000	Flanking Active TSS	NHEK	skin
49	chr20:25227000-25228400	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr20:25227000-25228600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin

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