Variant report

Variant	rs73135560
Chromosome Location	chr5:96696377-96696378
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:41398650..41400853-chr5:96695801..96698804,5	K562	blood:
2	chr5:96695823..96698804-chr6:142366314..142367822,2	K562	blood:
3	chr17:41463734..41465366-chr5:96695802..96697324,2	MCF-7	breast:
4	chr17:41462273..41467084-chr5:96695804..96698803,5	K562	blood:
5	chr17:41398605..41400432-chr5:96695803..96698802,4	MCF-7	breast:
6	chr17:41380186..41382311-chr5:96695804..96697321,3	MCF-7	breast:
7	chr17:41398860..41401971-chr5:96695801..96698802,6	K562	blood:
8	chr17:41380182..41383606-chr5:96695801..96698822,3	K562	blood:
9	chr17:41380182..41383629-chr5:96695802..96698822,5	K562	blood:

No data

Variant related genes	Relation type
ENSG00000236383	Chromatin interaction
ENSG00000188825	Chromatin interaction

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11949299	1.00[AMR][1000 genomes]
rs11949481	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11949589	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11949906	1.00[AMR][1000 genomes]
rs11949978	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11950055	1.00[AMR][1000 genomes]
rs11950085	1.00[AMR][1000 genomes]
rs11950117	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11950316	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11950486	1.00[AMR][1000 genomes]
rs11952283	0.90[AMR][1000 genomes]
rs11953093	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11954432	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11958643	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11958872	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11959208	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11960675	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17082251	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17087490	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58023467	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58234144	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59220198	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59393978	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61310706	0.81[AMR][1000 genomes]
rs61454257	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73137230	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73137235	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73137244	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73150774	0.90[AMR][1000 genomes]
rs7734072	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv1019790	chr5:96471680-96980633	Weak transcription ZNF genes & repeats Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv537812	chr5:96471680-96980633	ZNF genes & repeats Enhancers Flanking Active TSS Genic enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
4	nsv534326	chr5:96531217-97283481	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv882394	chr5:96538585-97108559	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
6	nsv1032548	chr5:96565121-97046804	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
7	nsv537813	chr5:96565121-97046804	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv830415	chr5:96597763-96764157	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv598964	chr5:96612401-96705762	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1025654	chr5:96613448-96817528	ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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