Variant report

Variant	rs4657474
Chromosome Location	chr1:165687152-165687153
allele	A/G
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:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:165686828..165687747-chr1:165893999..165894616,2	MCF-7	breast:
2	chr1:165686841..165687811-chr1:165882955..165884387,12	MCF-7	breast:
3	chr1:165600176..165602147-chr1:165685075..165687323,2	MCF-7	breast:
4	chr1:165686848..165687386-chr1:165884199..165884871,2	K562	blood:
5	chr1:165686810..165687319-chr1:165897019..165897710,2	K562	blood:
6	chr1:165686907..165688202-chr1:165883135..165884063,6	MCF-7	breast:
7	chr1:165685761..165688091-chr1:165797394..165800120,2	K562	blood:
8	chr1:165685865..165687619-chr1:165796541..165799023,2	MCF-7	breast:
9	chr1:165686936..165687730-chr1:165893570..165894520,2	MCF-7	breast:
10	chr1:165686871..165688066-chr1:165840434..165841110,4	MCF-7	breast:
11	chr1:165686346..165688021-chr1:165883094..165884168,12	K562	blood:

No data

Variant related genes	Relation type
ENSG00000143183	Chromatin interaction
ENSG00000143198	Chromatin interaction
ENSG00000143179	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10800153	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10800154	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10800155	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10918274	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12133745	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12691499	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12691500	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1547725	0.80[AMR][1000 genomes]
rs2790049	0.95[EUR][1000 genomes]
rs2790052	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2790053	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2814471	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4233408	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4537525	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4603103	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4656460	0.80[AMR][1000 genomes]
rs4656461	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4657471	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4657472	0.96[AFR][1000 genomes];0.92[AMR][1000 genomes]
rs4657475	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs4657476	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4657477	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6426936	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6660601	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6662839	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6668108	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6668885	0.82[EUR][1000 genomes]
rs6696454	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7518099	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7524755	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7528177	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7555523	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756102	chr1:165652342-165877342	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv1011720	chr1:165669589-165802516	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Genic enhancers Active TSS Strong 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	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165684400-165687600	Enhancers	Liver	Liver
2	chr1:165685200-165687600	Enhancers	HepG2	liver
3	chr1:165685200-165695400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr1:165685200-165696600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr1:165685200-165721600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr1:165685400-165687400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr1:165685600-165705200	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr1:165687000-165695200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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