Variant report

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

rs_ID	r²[population]
rs10175844	0.82[ASN][1000 genomes]
rs10208040	0.91[ASN][1000 genomes]
rs1105118	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1105119	0.94[ASN][1000 genomes]
rs1517396	0.89[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1543164	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1543165	0.94[ASN][1000 genomes]
rs2176407	0.90[ASN][1000 genomes]
rs2420045	0.90[ASN][1000 genomes]
rs3860462	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4405788	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4852831	0.94[ASN][1000 genomes]
rs4852832	0.94[ASN][1000 genomes]
rs4852833	0.92[ASN][1000 genomes]
rs4852836	0.84[ASN][1000 genomes]
rs4852838	0.83[ASN][1000 genomes]
rs6726291	0.95[ASN][1000 genomes]
rs7572229	0.92[ASN][1000 genomes]
rs7594591	0.84[ASN][1000 genomes]
rs7598575	0.92[ASN][1000 genomes]
rs883311	0.93[ASN][1000 genomes]
rs883312	0.94[ASN][1000 genomes]
rs908612	0.94[ASN][1000 genomes]
rs955788	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs955789	0.94[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:72227800-72235800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:72232400-72235600	Weak transcription	Esophagus	oesophagus
3	chr2:72232600-72240600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:72233600-72234600	Enhancers	Fetal Intestine Large	intestine
5	chr2:72233600-72235200	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr2:72233800-72234600	Enhancers	Fetal Intestine Small	intestine
7	chr2:72233800-72235600	Enhancers	Fetal Muscle Leg	muscle
8	chr2:72233800-72237600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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