Variant report

Variant	rs1388136
Chromosome Location	chr5:107033531-107033532
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:107016859..107019087-chr5:107031828..107034099,2	MCF-7	breast:
2	chr5:107023431..107026443-chr5:107031056..107034359,3	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1352726	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1363870	0.86[CHB][hapmap]
rs1388135	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1490836	0.95[ASN][1000 genomes]
rs149382	0.86[CHB][hapmap]
rs154191	0.86[CHB][hapmap]
rs164691	0.86[CHB][hapmap]
rs164693	0.86[CHB][hapmap]
rs164694	0.86[CHB][hapmap]
rs164837	0.86[CHB][hapmap]
rs17351329	0.82[ASN][1000 genomes]
rs26728	0.86[CHB][hapmap]
rs26729	0.86[CHB][hapmap]
rs26730	0.86[CHB][hapmap]
rs27550	0.86[CHB][hapmap];0.81[GIH][hapmap]
rs352602	0.86[CHB][hapmap]
rs35419	0.86[CHB][hapmap]
rs35533	0.86[CHB][hapmap]
rs42449	0.86[CHB][hapmap]
rs4588579	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4957712	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4957713	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4957714	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs59961335	0.95[ASN][1000 genomes]
rs62357932	0.95[ASN][1000 genomes]
rs62357937	0.95[ASN][1000 genomes]
rs62357940	0.86[ASN][1000 genomes]
rs67843712	0.84[ASN][1000 genomes]
rs6887589	0.82[CHD][hapmap]
rs723798	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73200677	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73200681	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73200683	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73202711	0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7444469	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34018	chr5:106720912-107110506	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107032400-107049000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr5:107032800-107035000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr5:107032800-107037800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr5:107032800-107040600	Weak transcription	H1 Cell Line	embryonic stem cell
5	chr5:107033000-107033800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr5:107033000-107040600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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