Variant report

Variant	rs73903922
Chromosome Location	chr20:24761581-24761582
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:24760897..24762927-chr20:24971923..24974297,2	MCF-7	breast:
2	chr20:24755822..24758667-chr20:24759812..24761777,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000101474	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs55760035	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58684827	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59252648	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59901088	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60531117	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61350955	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7270151	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7272053	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7272507	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7274081	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903587	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903589	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903916	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903917	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903918	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903919	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903920	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903921	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903923	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903924	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903926	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903927	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903929	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903930	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903931	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903932	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903933	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903934	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903935	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903936	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903937	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903939	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903940	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903942	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903944	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903945	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903946	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903948	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903950	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73903969	0.90[AMR][1000 genomes]
rs73903971	0.90[AMR][1000 genomes]
rs73903972	0.90[AMR][1000 genomes]
rs73903974	0.90[AMR][1000 genomes]
rs73903977	0.90[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332519	chr20:24535099-24815615	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1061412	chr20:24629468-24887869	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv544216	chr20:24629468-24887869	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1061281	chr20:24711635-24815107	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv544217	chr20:24711635-24815107	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv912825	chr20:24715544-24813345	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv1061455	chr20:24733120-24861801	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv544218	chr20:24733120-24861801	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv1059270	chr20:24741923-24787243	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24749200-24763600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr20:24757800-24766600	Enhancers	Fetal Thymus	thymus
3	chr20:24758400-24766800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr20:24758600-24762400	Enhancers	Primary hematopoietic stem cells	blood
5	chr20:24758600-24763800	Enhancers	Fetal Muscle Leg	muscle
6	chr20:24758800-24762400	Enhancers	Thymus	Thymus
7	chr20:24758800-24767400	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr20:24759800-24761600	Weak transcription	Colon Smooth Muscle	Colon
9	chr20:24759800-24761800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr20:24759800-24761800	Weak transcription	Fetal Brain Female	brain
11	chr20:24759800-24767000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr20:24760800-24761600	Active TSS	Spleen	Spleen
13	chr20:24760800-24761800	Enhancers	Primary B cells from peripheral blood	blood
14	chr20:24760800-24761800	Weak transcription	Fetal Lung	lung
15	chr20:24761000-24762800	Enhancers	Stomach Smooth Muscle	stomach
16	chr20:24761200-24761800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr20:24761200-24761800	Enhancers	Dnd41	blood
18	chr20:24761200-24762200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr20:24761200-24762400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr20:24761200-24762400	Enhancers	Brain Inferior Temporal Lobe	brain
21	chr20:24761200-24763400	Enhancers	Brain Substantia Nigra	brain
22	chr20:24761400-24761800	Enhancers	Brain Angular Gyrus	brain
23	chr20:24761400-24762400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr20:24761400-24764000	Enhancers	Brain Hippocampus Middle	brain
25	chr20:24761400-24765200	Weak transcription	Primary T cells from cord blood	blood

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