Variant report

Variant	rs73121277
Chromosome Location	chr7:50577968-50577969
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IKZF1-7	chr7:50577437-50578655	refGeneNc_4230_NR_033845

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

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10239937	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10244632	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10249982	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10274275	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12535064	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12538830	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1451366	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1451368	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1901311	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1901312	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1982406	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2100280	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2122818	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2122821	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2167366	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4947588	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4947589	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6592963	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6592973	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6952023	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6963534	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6967361	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6970468	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6974583	0.92[AMR][1000 genomes];0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7797142	0.81[AMR][1000 genomes]
rs7807564	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9918591	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9918702	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016665	chr7:50452552-51404524	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv888021	chr7:50538589-50610071	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1015758	chr7:50565404-50768153	Flanking Active TSS Genic enhancers Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
4	nsv1023228	chr7:50573214-50777634	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:50543600-50595000	Weak transcription	Liver	Liver
2	chr7:50560800-50581000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr7:50565200-50609000	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr7:50566200-50581200	Strong transcription	Fetal Intestine Small	intestine
5	chr7:50569000-50592800	Weak transcription	HepG2	liver
6	chr7:50571000-50580200	Weak transcription	Pancreas	Pancrea
7	chr7:50571000-50582400	Weak transcription	Right Atrium	heart
8	chr7:50575400-50578000	Strong transcription	Fetal Intestine Large	intestine
9	chr7:50576600-50580800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr7:50576600-50581000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:50577000-50580200	Weak transcription	K562	blood
12	chr7:50577000-50581600	Weak transcription	Duodenum Mucosa	Duodenum
13	chr7:50577000-50583400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr7:50577400-50580600	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr7:50577400-50581000	Weak transcription	Skeletal Muscle Male	skeletal muscle

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