Variant report

Variant	rs10135283
Chromosome Location	chr14:97252629-97252630
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:97250880..97254432-chr14:97261581..97265301,4	K562	blood:
2	chr14:97252075..97254821-chr14:97254880..97257598,2	K562	blood:
3	chr14:97246983..97249194-chr14:97251275..97253607,2	K562	blood:
4	chr14:97251859..97256627-chr14:97261114..97265301,5	K562	blood:

Variant related genes	Relation type
ENSG00000100749	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 3 )

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

rs_ID	r²[population]
rs10131890	0.86[JPT][hapmap]
rs10132573	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10135222	0.82[CHD][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs10135234	1.00[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.88[LWK][hapmap];0.91[MEX][hapmap];0.82[MKK][hapmap];0.85[TSI][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10144908	0.81[ASN][1000 genomes]
rs10145396	0.82[CHD][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs11160369	0.82[CHB][hapmap]
rs11628733	0.82[CHB][hapmap]
rs12587775	0.80[ASN][1000 genomes]
rs12878184	0.84[CHD][hapmap]
rs12882176	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12883251	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs17310204	0.87[JPT][hapmap]
rs1957134	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1957135	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.95[MEX][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2145636	0.88[CHD][hapmap]
rs2145638	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2145639	0.81[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs2224442	0.82[CHB][hapmap]
rs2230532	0.81[CHD][hapmap]
rs4633647	0.88[ASN][1000 genomes]
rs4900345	0.83[ASN][1000 genomes]
rs61980999	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7160250	0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs723810	0.81[CHD][hapmap]
rs8009190	0.83[ASN][1000 genomes]
rs912340	0.86[ASN][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	nsv1041078	chr14:97001679-97279220	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1050075	chr14:97004951-97279220	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
3	nsv1044202	chr14:97155291-97683983	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv542179	chr14:97155291-97683983	Weak transcription Strong transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv510650	chr14:97238489-97325221	Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs10135283	TCL1A	cis	cerebellum	SCAN
rs10135283	SCARNA13	cis	cerebellum	SCAN
rs10135283	VRK1	cis	parietal	SCAN

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:97250200-97254400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr14:97251400-97253400	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr14:97252200-97255000	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr14:97252600-97254800	Weak transcription	Primary monocytes fromperipheralblood	blood

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