Variant report

Variant	rs28600205
Chromosome Location	chr4:643968-643969
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:641525..644066-chr4:652058..654958,2	K562	blood:
2	chr4:640899..644048-chr4:645918..649470,4	K562	blood:
3	chr4:636743..639513-chr4:642400..644519,2	MCF-7	breast:
4	chr4:642830..644425-chr4:665822..667972,2	K562	blood:
5	chr4:642131..644821-chr4:649750..652284,2	MCF-7	breast:
6	chr4:642255..644273-chr4:662905..665187,2	K562	blood:
7	chr4:642559..644121-chr4:666907..669790,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000133256	Chromatin interaction
ENSG00000242686	Chromatin interaction
ENSG00000169020	Chromatin interaction
ENSG00000215375	Chromatin interaction

Extended variants
information (count: 73 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs10007206	0.93[ASN][1000 genomes]
rs10007497	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10011154	0.95[ASN][1000 genomes]
rs10023472	0.99[ASN][1000 genomes]
rs10027866	0.99[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10029928	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10031745	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10031968	0.82[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10033239	0.83[AFR][1000 genomes]
rs11248029	0.87[ASN][1000 genomes]
rs13107358	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28374488	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28380593	0.91[ASN][1000 genomes]
rs28403281	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28438498	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28476575	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28502612	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28504161	0.85[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs28520978	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28568555	0.93[AFR][1000 genomes]
rs28588872	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28630797	0.91[AFR][1000 genomes]
rs28714509	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28754797	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28769407	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28826275	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs34307246	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs3864130	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3864131	0.90[AFR][1000 genomes]
rs3888807	0.95[ASN][1000 genomes]
rs3934459	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4075653	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4505760	1.00[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs59623849	0.92[ASN][1000 genomes]
rs60316402	0.83[AFR][1000 genomes]
rs67030464	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs67703486	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs71602496	0.93[AFR][1000 genomes]
rs72611195	0.80[ASN][1000 genomes]
rs72611197	0.86[ASN][1000 genomes]
rs72611198	0.87[ASN][1000 genomes]
rs72611199	0.87[ASN][1000 genomes]
rs72611200	0.87[ASN][1000 genomes]
rs72611201	0.87[ASN][1000 genomes]
rs72611202	0.87[ASN][1000 genomes]
rs72613103	0.87[ASN][1000 genomes]
rs72613104	0.93[ASN][1000 genomes]
rs72613105	0.93[ASN][1000 genomes]
rs72613106	0.93[ASN][1000 genomes]
rs72613107	0.92[ASN][1000 genomes]
rs72613108	0.99[ASN][1000 genomes]
rs7438471	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7661376	0.82[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9884240	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9992641	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9997286	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9998967	0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1011715	chr4:43860-823487	Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
2	esv2830422	chr4:72247-681939	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
3	nsv931097	chr4:72447-683874	Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
4	nsv532702	chr4:72447-755236	Active TSS ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
5	nsv1005224	chr4:507005-900281	Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Strong transcription Weak transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv536976	chr4:507005-900281	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
7	nsv878245	chr4:509178-694613	Active TSS Flanking Active TSS Enhancers Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv822425	chr4:540105-1413799	Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	108 gene(s)	inside rSNPs	diseases
9	nsv878246	chr4:592507-696848	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
10	esv2757916	chr4:603208-931354	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
11	esv2759217	chr4:603208-931354	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
12	nsv878247	chr4:607202-925149	Bivalent Enhancer Flanking Active TSS Strong transcription Bivalent/Poised TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
13	nsv530490	chr4:614355-1399150	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
14	nsv593206	chr4:625962-735150	Weak transcription Flanking Active TSS Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
15	nsv593207	chr4:629437-645300	Bivalent/Poised TSS Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
16	nsv4194	chr4:635316-657212	Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:631400-657000	Weak transcription	Right Atrium	heart
2	chr4:640400-648400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:641800-657000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr4:642200-652800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr4:642400-654600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr4:642600-645000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr4:642800-644600	Weak transcription	Gastric	stomach
8	chr4:642800-657000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:643000-646000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr4:643000-657000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr4:643200-646200	Bivalent Enhancer	Fetal Muscle Leg	muscle
12	chr4:643200-648200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:643400-644600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:643600-644400	Bivalent Enhancer	Brain Hippocampus Middle	brain
15	chr4:643600-644600	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr4:643800-644400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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