Variant report

Variant	rs55809585
Chromosome Location	chr5:60103598-60103599
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:60098668..60100244-chr5:60103216..60104950,2	K562	blood:
2	chr5:60096040..60098650-chr5:60101682..60104091,2	K562	blood:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10057395	0.82[ASN][1000 genomes]
rs10062839	0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs10072745	0.82[ASN][1000 genomes]
rs10076679	0.87[ASN][1000 genomes]
rs10077663	0.89[ASN][1000 genomes]
rs13184554	0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1445292	0.84[AMR][1000 genomes]
rs1824531	0.88[EUR][1000 genomes]
rs1870015	0.82[ASN][1000 genomes]
rs35006499	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs36111624	0.89[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs4235481	0.87[ASN][1000 genomes]
rs4235482	0.87[ASN][1000 genomes]
rs4410607	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4479795	0.87[AMR][1000 genomes]
rs4482855	0.89[ASN][1000 genomes]
rs4700392	0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4700393	0.91[ASN][1000 genomes]
rs6449500	0.82[ASN][1000 genomes]
rs6449501	0.87[ASN][1000 genomes]
rs6449502	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6449503	0.83[ASN][1000 genomes]
rs6449504	0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs6449505	0.83[AMR][1000 genomes]
rs6869332	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6871557	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6872863	0.82[ASN][1000 genomes]
rs6873181	0.82[ASN][1000 genomes]
rs6875456	0.87[ASN][1000 genomes]
rs6876335	0.87[ASN][1000 genomes]
rs6876346	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6877757	0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6877849	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6889730	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6890201	0.87[ASN][1000 genomes]
rs6894672	0.82[ASN][1000 genomes]
rs6894750	0.87[ASN][1000 genomes]
rs6894795	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7712473	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7714071	0.86[EUR][1000 genomes]
rs7730827	0.89[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs921897	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv492277	chr5:59905195-60180834	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv462198	chr5:59969015-60116613	Strong transcription Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv598298	chr5:59969015-60116613	ZNF genes & repeats Flanking Active TSS Enhancers Weak transcription Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv934153	chr5:60004982-60309751	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription 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 target site	15 gene(s)	inside rSNPs	diseases
5	esv2763456	chr5:60007355-60151767	Bivalent Enhancer Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
6	nsv1026190	chr5:60020156-60148535	Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Enhancers ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
7	nsv537769	chr5:60020156-60148535	Weak transcription Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	5 gene(s)	inside rSNPs	diseases
8	esv2752073	chr5:60034475-60136626	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	3 gene(s)	inside rSNPs	diseases
9	nsv949662	chr5:60047974-60488379	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
10	nsv1017095	chr5:60050600-60414783	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
11	nsv933326	chr5:60074031-60413061	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60082400-60112600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr5:60091200-60104200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr5:60091400-60105200	Weak transcription	K562	blood
4	chr5:60092800-60110400	Weak transcription	Brain Substantia Nigra	brain
5	chr5:60101800-60105800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr5:60101800-60105800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr5:60101800-60105800	Weak transcription	NHEK	skin
8	chr5:60101800-60106000	Weak transcription	HMEC	breast
9	chr5:60102000-60106000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr5:60102200-60137800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr5:60102800-60105800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr5:60103000-60110200	Weak transcription	Fetal Intestine Large	intestine
13	chr5:60103000-60125600	Weak transcription	Brain Angular Gyrus	brain
14	chr5:60103000-60129000	Weak transcription	Fetal Intestine Small	intestine
15	chr5:60103400-60111800	Weak transcription	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links