Variant report

Variant	rs72727908
Chromosome Location	chr4:147024985-147024986
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs12508201	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12511944	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs72727907	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs72727916	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147021000-147026400	Weak transcription	Rectal Mucosa Donor 29	rectum
2	chr4:147021200-147026000	Weak transcription	Fetal Intestine Small	intestine
3	chr4:147021200-147029000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:147022400-147025600	Weak transcription	GM12878-XiMat	blood
5	chr4:147024400-147025400	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr4:147024400-147025800	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr4:147024600-147035000	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr4:147024800-147025000	Enhancers	Primary B cells from cord blood	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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