Variant report

Variant	rs1199960
Chromosome Location	chr13:37668008-37668009
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:71)

rs_ID	r²[population]
rs1199951	0.90[EUR][1000 genomes]
rs1199956	0.88[EUR][1000 genomes]
rs1199962	0.82[EUR][1000 genomes]
rs1199963	0.94[TSI][hapmap];0.88[EUR][1000 genomes]
rs1199972	0.87[EUR][1000 genomes]
rs1199974	0.84[EUR][1000 genomes]
rs1199977	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1199978	0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1199979	0.90[EUR][1000 genomes]
rs1199980	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1199981	0.86[EUR][1000 genomes]
rs1199982	0.94[TSI][hapmap];0.86[EUR][1000 genomes]
rs1199984	0.94[TSI][hapmap];0.87[EUR][1000 genomes]
rs1199986	0.90[EUR][1000 genomes]
rs1199987	0.90[EUR][1000 genomes]
rs1199988	0.88[EUR][1000 genomes]
rs1199989	0.88[EUR][1000 genomes]
rs1336755	0.88[EUR][1000 genomes]
rs1543738	0.87[TSI][hapmap];0.83[EUR][1000 genomes]
rs17054795	0.95[LWK][hapmap]
rs17054810	1.00[YRI][hapmap]
rs1764481	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1764483	0.94[TSI][hapmap];0.86[EUR][1000 genomes]
rs1764484	0.87[EUR][1000 genomes]
rs1764486	0.90[EUR][1000 genomes]
rs1764487	0.88[EUR][1000 genomes]
rs1764488	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1924418	0.84[EUR][1000 genomes]
rs1924422	0.81[TSI][hapmap]
rs1924426	0.86[EUR][1000 genomes]
rs1937760	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2093817	0.94[TSI][hapmap];0.84[EUR][1000 genomes]
rs2147169	0.87[TSI][hapmap]
rs2211618	0.88[EUR][1000 genomes]
rs2323165	0.87[TSI][hapmap]
rs2669893	0.88[EUR][1000 genomes]
rs2785620	0.87[TSI][hapmap];0.84[EUR][1000 genomes]
rs2997189	0.87[EUR][1000 genomes]
rs2997190	0.90[EUR][1000 genomes]
rs2997193	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3858859	0.83[EUR][1000 genomes]
rs4291799	0.87[TSI][hapmap]
rs4941854	0.87[TSI][hapmap]
rs4941856	0.87[TSI][hapmap]
rs4943441	0.93[TSI][hapmap]
rs6563507	0.87[TSI][hapmap]
rs6563508	0.94[TSI][hapmap];0.86[EUR][1000 genomes]
rs6563509	0.84[EUR][1000 genomes]
rs73175079	0.80[EUR][1000 genomes]
rs7317750	0.87[TSI][hapmap]
rs7320899	0.84[EUR][1000 genomes]
rs7321129	0.81[TSI][hapmap]
rs7326688	0.88[EUR][1000 genomes]
rs7338929	0.87[TSI][hapmap]
rs7339296	0.86[EUR][1000 genomes]
rs7983986	0.87[TSI][hapmap]
rs7989205	0.87[TSI][hapmap]
rs7989380	0.88[EUR][1000 genomes]
rs7995098	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7997310	0.94[TSI][hapmap];0.84[EUR][1000 genomes]
rs8001662	0.84[EUR][1000 genomes]
rs9532001	0.81[TSI][hapmap]
rs9532004	0.81[TSI][hapmap]
rs9532005	0.87[TSI][hapmap]
rs9547707	0.81[TSI][hapmap]
rs9547715	0.87[TSI][hapmap]
rs9547718	0.87[TSI][hapmap]
rs9547721	0.86[EUR][1000 genomes]
rs9547725	0.87[EUR][1000 genomes]
rs9576162	0.88[EUR][1000 genomes]
rs9603121	0.81[TSI][hapmap]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948975	chr13:37281203-38280430	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1199960	SUPT20H	cis	Whole Blood	GTEx

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:37665000-37668200	Active TSS	Primary B cells from cord blood	blood
2	chr13:37665400-37678400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr13:37666200-37669200	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr13:37666600-37668800	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr13:37667800-37669400	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
6	chr13:37668000-37668200	Enhancers	Fetal Muscle Leg	muscle
7	chr13:37668000-37668600	Enhancers	Fetal Lung	lung
8	chr13:37668000-37668600	Enhancers	Fetal Stomach	stomach

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