Variant report

Variant	rs60281617
Chromosome Location	chr8:68308189-68308190
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs12677893	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56762242	0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61052740	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61702591	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs66993446	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7015159	0.90[ASN][1000 genomes]
rs7829537	0.97[EUR][1000 genomes];0.97[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	esv2752263	chr8:68170946-68788493	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	esv1839724	chr8:68195817-68346693	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv1024135	chr8:68235792-68629789	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv539642	chr8:68235792-68629789	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	esv2752264	chr8:68244546-68647201	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 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	chr8:68283400-68314000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:68306000-68308800	Enhancers	Primary T cells from cord blood	blood
3	chr8:68307000-68308200	Weak transcription	Fetal Thymus	thymus
4	chr8:68307000-68312200	Weak transcription	Primary T cells fromperipheralblood	blood
5	chr8:68307400-68312600	Weak transcription	Primary hematopoietic stem cells	blood
6	chr8:68307600-68312400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr8:68307800-68312600	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr8:68307800-68312600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr8:68307800-68313200	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr8:68308000-68308200	Enhancers	Thymus	Thymus
11	chr8:68308000-68310800	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr8:68308000-68310800	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr8:68308000-68311800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr8:68308000-68312000	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr8:68308000-68312600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr8:68308000-68312600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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