Variant report

Variant	rs4704202
Chromosome Location	chr5:74574324-74574325
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10070119	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10942734	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11957260	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1423527	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2112653	0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2126736	0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2335418	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4704200	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6892023	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7702895	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7722186	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[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	nsv1016610	chr5:74403611-74627654	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv2758000	chr5:74433760-74611714	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2759350	chr5:74433760-74611714	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:74568400-74579400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr5:74570400-74576200	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr5:74572000-74581600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr5:74573000-74575200	Enhancers	Pancreatic Islets	Pancreatic Islet
5	chr5:74573600-74577600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr5:74573600-74578400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr5:74573800-74577600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr5:74574000-74577600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr5:74574200-74574800	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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

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