Variant report

Variant	rs6865374
Chromosome Location	chr5:2200150-2200151
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr5:2194335..2197106-chr5:2198597..2201677,3	K562	blood:
2	chr5:2196715..2198359-chr5:2200115..2201772,2	MCF-7	breast:
3	chr5:2199358..2202641-chr5:2202750..2204826,3	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10053297	0.94[ASN][1000 genomes]
rs10059122	0.91[ASN][1000 genomes]
rs10078052	0.87[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10462752	0.80[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs11133933	0.94[ASN][1000 genomes]
rs11133935	0.89[AFR][1000 genomes]
rs11133936	0.94[AFR][1000 genomes]
rs11741534	0.97[ASN][1000 genomes]
rs11747063	0.90[AFR][1000 genomes]
rs12189415	0.99[ASN][1000 genomes]
rs13156721	0.96[ASN][1000 genomes]
rs13157950	0.99[ASN][1000 genomes]
rs13172851	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs13176661	0.98[ASN][1000 genomes]
rs13181974	0.98[ASN][1000 genomes]
rs13186652	0.98[ASN][1000 genomes]
rs17584572	0.95[ASN][1000 genomes]
rs2405802	0.84[AFR][1000 genomes]
rs4866475	0.82[ASN][1000 genomes]
rs4866649	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4866652	0.97[ASN][1000 genomes]
rs6555069	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs6555070	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6555071	0.93[ASN][1000 genomes]
rs6879173	0.82[ASN][1000 genomes]
rs6893234	0.82[ASN][1000 genomes]
rs9312987	0.84[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869236	chr5:1719263-2259100	Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	66 gene(s)	inside rSNPs	diseases
2	nsv880947	chr5:2146761-2251313	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv881232	chr5:2150273-2213762	ZNF genes & repeats Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv880789	chr5:2159490-2213762	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv596908	chr5:2186956-2254295	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:2197800-2200200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr5:2198600-2200600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr5:2198600-2200800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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