Variant report

Variant	rs11097619
Chromosome Location	chr4:99452423-99452424
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10002696	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10006366	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10006430	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10025051	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13108940	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13123700	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1528547	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs1919210	0.86[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2037832	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28886705	0.81[ASN][1000 genomes]
rs4447870	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4699343	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4699344	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4699345	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs4699348	0.88[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4699639	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4699640	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4699644	0.96[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4699646	0.84[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs4699648	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6815038	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6823547	0.86[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs6847124	0.90[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs71600251	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs9760870	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529623	chr4:98501338-99460166	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
2	esv2754250	chr4:99094922-99527122	Strong transcription Flanking Active TSS Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1004181	chr4:99208152-99529576	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99440400-99458400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:99445200-99461800	Weak transcription	HMEC	breast
3	chr4:99445400-99465400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr4:99446000-99467400	Weak transcription	Fetal Stomach	stomach
5	chr4:99446800-99457400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr4:99446800-99461600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr4:99448200-99461000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:99449400-99461200	Weak transcription	NHEK	skin
9	chr4:99449400-99464200	Weak transcription	Fetal Brain Female	brain
10	chr4:99449800-99467400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr4:99450200-99458400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:99450200-99467400	Weak transcription	Osteobl	bone
13	chr4:99450400-99461800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr4:99450400-99465200	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr4:99450800-99458800	Weak transcription	NHLF	lung
16	chr4:99450800-99468000	Weak transcription	HSMM	muscle
17	chr4:99451200-99457000	Weak transcription	Cortex derived primary cultured neurospheres	brain
18	chr4:99451600-99458800	Weak transcription	Brain Hippocampus Middle	brain
19	chr4:99451800-99457000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr4:99451800-99457200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr4:99451800-99457400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:99451800-99458200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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