Variant report

Variant	rs1447367
Chromosome Location	chr4:30848135-30848136
allele	C/G/T
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:26)

rs_ID	r²[population]
rs10003247	0.88[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10517215	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12643430	0.86[AFR][1000 genomes]
rs1374653	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1374656	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1447366	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1447369	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1447374	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16884125	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2310224	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34280337	0.86[AFR][1000 genomes]
rs34317883	0.86[AFR][1000 genomes]
rs35154721	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35580687	0.86[AFR][1000 genomes]
rs4359861	0.86[AFR][1000 genomes]
rs4692486	0.86[AFR][1000 genomes]
rs6820105	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6820251	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72619194	0.86[AFR][1000 genomes]
rs72619195	0.86[AFR][1000 genomes]
rs72619196	0.86[AFR][1000 genomes]
rs72619197	0.86[AFR][1000 genomes]
rs72619198	0.86[AFR][1000 genomes]
rs72619199	0.86[AFR][1000 genomes]
rs73121566	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73121588	0.88[AMR][1000 genomes];0.87[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	nsv878810	chr4:30823157-30987395	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
2	nsv998450	chr4:30823631-31628179	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:30838800-30848600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:30839200-30848600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr4:30840600-30848400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:30841400-30849800	Weak transcription	Colon Smooth Muscle	Colon
5	chr4:30842000-30854400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:30842400-30849000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr4:30842400-30855200	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr4:30842600-30848400	Weak transcription	Fetal Lung	lung
9	chr4:30842600-30854600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr4:30842600-30855800	Weak transcription	Aorta	Aorta
11	chr4:30844400-30850200	Weak transcription	Fetal Heart	heart
12	chr4:30846600-30848200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr4:30846600-30848400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr4:30846600-30855000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr4:30846800-30848200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr4:30846800-30854600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:30847000-30848200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr4:30847000-30848400	Weak transcription	Fetal Muscle Leg	muscle
19	chr4:30847000-30851000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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