Variant report

Variant	rs71464100
Chromosome Location	chr11:73662835-73662836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:73661884..73663494-chr11:73691354..73693894,2	MCF-7	breast:
2	chr11:73662123..73663780-chr11:73665795..73667370,2	K562	blood:
3	chr11:73662160..73664087-chr11:73665599..73668427,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000175567	Chromatin interaction

Extended variants
information (count: 148 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:146)

rs_ID	r²[population]
rs1051090	0.84[AMR][1000 genomes]
rs12786008	0.84[AMR][1000 genomes]
rs12786020	0.84[AMR][1000 genomes]
rs12786118	0.84[AMR][1000 genomes]
rs12786752	0.87[AMR][1000 genomes]
rs12787838	0.87[AMR][1000 genomes]
rs12789142	0.84[AMR][1000 genomes]
rs12790445	0.84[AMR][1000 genomes]
rs12790985	0.92[AMR][1000 genomes]
rs12791467	0.84[AMR][1000 genomes]
rs12791617	0.84[AMR][1000 genomes]
rs12791811	0.84[AMR][1000 genomes]
rs12792711	0.84[AMR][1000 genomes]
rs12793053	0.82[AMR][1000 genomes]
rs12793342	0.83[AMR][1000 genomes]
rs12793550	0.83[AMR][1000 genomes]
rs12793555	0.84[AMR][1000 genomes]
rs12793757	0.84[AMR][1000 genomes]
rs12793826	0.84[AMR][1000 genomes]
rs12794180	0.84[AMR][1000 genomes]
rs12795932	0.84[AMR][1000 genomes]
rs12798393	0.84[AMR][1000 genomes]
rs12799686	0.84[AMR][1000 genomes]
rs12799720	0.92[AMR][1000 genomes]
rs12799764	0.85[AMR][1000 genomes]
rs12799849	0.84[AMR][1000 genomes]
rs12801268	0.84[AMR][1000 genomes]
rs12801553	0.84[AMR][1000 genomes]
rs12801713	0.84[AMR][1000 genomes]
rs12804010	0.84[AMR][1000 genomes]
rs12804029	0.84[AMR][1000 genomes]
rs12804511	0.92[AMR][1000 genomes]
rs12808007	0.84[AMR][1000 genomes]
rs12808395	0.84[AMR][1000 genomes]
rs1641	0.84[AMR][1000 genomes]
rs17310423	0.84[AMR][1000 genomes]
rs34095255	0.84[AMR][1000 genomes]
rs34217459	0.84[AMR][1000 genomes]
rs34243263	0.84[AMR][1000 genomes]
rs34258880	0.84[AMR][1000 genomes]
rs34308910	0.84[AMR][1000 genomes]
rs34433535	0.84[AMR][1000 genomes]
rs34475888	0.84[AMR][1000 genomes]
rs34476415	0.84[AMR][1000 genomes]
rs34550191	0.84[AMR][1000 genomes]
rs34572223	0.83[AMR][1000 genomes]
rs34578576	0.84[AMR][1000 genomes]
rs34590823	0.85[AMR][1000 genomes]
rs34659829	0.84[AMR][1000 genomes]
rs34664984	0.92[AMR][1000 genomes]
rs34671213	0.82[AMR][1000 genomes]
rs34771588	0.84[AMR][1000 genomes]
rs34793574	0.84[AMR][1000 genomes]
rs34828254	0.84[AMR][1000 genomes]
rs34840689	0.80[AMR][1000 genomes]
rs34932908	0.84[AMR][1000 genomes]
rs35066247	0.84[AMR][1000 genomes]
rs35079634	0.83[AMR][1000 genomes]
rs35123949	0.84[AMR][1000 genomes]
rs35130893	0.83[AMR][1000 genomes]
rs35208638	0.84[AMR][1000 genomes]
rs35235512	0.83[AMR][1000 genomes]
rs35248853	0.84[AMR][1000 genomes]
rs35277500	0.92[AMR][1000 genomes]
rs35314844	0.84[AMR][1000 genomes]
rs35320080	0.84[AMR][1000 genomes]
rs35344902	0.84[AMR][1000 genomes]
rs35349379	0.92[AMR][1000 genomes]
rs35414679	0.92[AMR][1000 genomes]
rs35481171	0.84[AMR][1000 genomes]
rs35506086	0.84[AMR][1000 genomes]
rs35598792	0.84[AMR][1000 genomes]
rs35640394	0.84[AMR][1000 genomes]
rs35645696	0.84[AMR][1000 genomes]
rs35683504	0.84[AMR][1000 genomes]
rs35741071	0.84[AMR][1000 genomes]
rs35852922	0.84[AMR][1000 genomes]
rs35876082	0.92[AMR][1000 genomes]
rs35976844	0.84[AMR][1000 genomes]
rs35991676	0.84[AMR][1000 genomes]
rs36004107	0.84[AMR][1000 genomes]
rs36011596	0.87[AMR][1000 genomes]
rs36034275	0.84[AMR][1000 genomes]
rs36076594	0.84[AMR][1000 genomes]
rs3758930	0.84[AMR][1000 genomes]
rs55677926	0.84[AMR][1000 genomes]
rs55740271	0.84[AMR][1000 genomes]
rs55788830	0.92[AMR][1000 genomes]
rs55798481	0.92[AMR][1000 genomes]
rs55850940	0.84[AMR][1000 genomes]
rs55987259	0.84[AMR][1000 genomes]
rs56034488	0.92[AMR][1000 genomes]
rs56159953	0.91[AMR][1000 genomes]
rs56186807	0.92[AMR][1000 genomes]
rs57736748	0.84[AMR][1000 genomes]
rs58199491	0.84[AMR][1000 genomes]
rs60918915	0.84[AMR][1000 genomes]
rs6592539	0.84[AMR][1000 genomes]
rs6592540	0.84[AMR][1000 genomes]
rs6592541	0.84[AMR][1000 genomes]
rs7105778	0.84[AMR][1000 genomes]
rs7113309	0.84[AMR][1000 genomes]
rs7114235	0.96[AMR][1000 genomes]
rs7114340	0.92[AMR][1000 genomes]
rs7119014	0.84[AMR][1000 genomes]
rs7119242	0.84[AMR][1000 genomes]
rs7122091	0.96[AMR][1000 genomes]
rs7122397	0.84[AMR][1000 genomes]
rs7123766	0.84[AMR][1000 genomes]
rs7124461	0.84[AMR][1000 genomes]
rs7124674	0.84[AMR][1000 genomes]
rs71464087	0.84[AMR][1000 genomes]
rs71464088	0.87[AMR][1000 genomes]
rs71464089	0.84[AMR][1000 genomes]
rs71464091	0.84[AMR][1000 genomes]
rs71464094	0.80[AMR][1000 genomes]
rs71464096	0.84[AMR][1000 genomes]
rs71464098	0.92[AMR][1000 genomes]
rs71464099	0.92[AMR][1000 genomes]
rs71479550	0.83[AMR][1000 genomes]
rs71479553	0.84[AMR][1000 genomes]
rs71479554	0.84[AMR][1000 genomes]
rs71479555	0.84[AMR][1000 genomes]
rs71479561	0.84[AMR][1000 genomes]
rs71479562	0.84[AMR][1000 genomes]
rs71479563	0.84[AMR][1000 genomes]
rs71479564	0.84[AMR][1000 genomes]
rs71479565	0.84[AMR][1000 genomes]
rs7924403	0.80[AMR][1000 genomes]
rs7926863	0.84[AMR][1000 genomes]
rs7929572	0.84[AMR][1000 genomes]
rs7931475	0.83[AMR][1000 genomes]
rs7931833	0.84[AMR][1000 genomes]
rs7932961	0.84[AMR][1000 genomes]
rs7937179	0.84[AMR][1000 genomes]
rs7938019	0.83[AMR][1000 genomes]
rs7940614	0.87[AMR][1000 genomes]
rs7941476	0.84[AMR][1000 genomes]
rs7944702	0.84[AMR][1000 genomes]
rs7944901	0.84[AMR][1000 genomes]
rs7944908	0.84[AMR][1000 genomes]
rs7945614	0.84[AMR][1000 genomes]
rs7945891	0.83[AMR][1000 genomes]
rs7946245	0.84[AMR][1000 genomes]
rs7948076	0.84[AMR][1000 genomes]
rs7951088	0.84[AMR][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	nsv492091	chr11:73285970-73844424	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
2	nsv1038105	chr11:73552023-73673836	Strong transcription Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:73639400-73668000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr11:73640800-73667000	Weak transcription	Pancreas	Pancrea
3	chr11:73641400-73672200	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr11:73650200-73666800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr11:73650200-73667000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:73660600-73667000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:73662000-73663400	Active TSS	Brain Anterior Caudate	brain
8	chr11:73662000-73663600	Enhancers	Fetal Kidney	kidney
9	chr11:73662000-73663800	Enhancers	HSMM	muscle
10	chr11:73662000-73664000	Enhancers	HSMMtube	muscle
11	chr11:73662400-73667000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr11:73662400-73667000	Weak transcription	NH-A	brain
13	chr11:73662400-73668200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:73662600-73663000	Active TSS	HepG2	liver

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