Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:112315702..112318963-chr7:112319210..112322447,4	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10228483	0.83[EUR][1000 genomes]
rs10233896	0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10234058	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10242871	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10253054	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10261844	0.86[EUR][1000 genomes]
rs10269793	0.84[EUR][1000 genomes]
rs10273060	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10273589	0.84[EUR][1000 genomes]
rs10280916	0.85[EUR][1000 genomes]
rs1227155	0.84[EUR][1000 genomes]
rs1227163	0.84[EUR][1000 genomes]
rs1614000	0.85[EUR][1000 genomes]
rs1922907	0.82[ASN][1000 genomes]
rs2028028	0.89[ASN][1000 genomes]
rs2188551	0.82[AFR][1000 genomes]
rs2905274	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3734956	0.83[EUR][1000 genomes]
rs56113805	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs56376790	0.86[EUR][1000 genomes]
rs62475004	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6466419	0.85[EUR][1000 genomes]
rs6945635	0.82[ASN][1000 genomes]
rs6948876	0.84[EUR][1000 genomes]
rs6970266	0.82[ASN][1000 genomes]
rs7780098	0.81[AMR][1000 genomes];0.84[EUR][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	nsv531436	chr7:111856171-112585407	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	105 gene(s)	inside rSNPs	diseases
2	nsv889055	chr7:112174089-112353440	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr7:112310000-112317600	Weak transcription	Placenta	Placenta
2	chr7:112312800-112318200	Enhancers	iPS-18 Cell Line	embryonic stem cell
3	chr7:112312800-112319000	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr7:112313200-112319000	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr7:112313600-112317600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr7:112314200-112318200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr7:112315000-112317000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr7:112315000-112317600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr7:112315200-112316400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:112315800-112316400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr7:112316000-112317600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr7:112316200-112316600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:112316200-112318200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:112316200-112318200	Enhancers	HUES6 Cell Line	embryonic stem cell

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