Variant report

Variant	rs9949302
Chromosome Location	chr18:44128477-44128478
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12956234	0.85[AFR][1000 genomes];0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17768374	0.91[CEU][hapmap];1.00[CHB][hapmap];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34175594	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34693070	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41393146	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9945193	0.94[AFR][1000 genomes];0.88[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs9946967	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9947183	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9949102	1.00[CEU][hapmap];1.00[CHB][hapmap];0.83[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9956148	0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9967253	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44126600-44128800	Weak transcription	Colon Smooth Muscle	Colon
2	chr18:44126600-44130400	Weak transcription	Right Atrium	heart
3	chr18:44126600-44130600	Weak transcription	Primary neutrophils fromperipheralblood	blood
4	chr18:44126600-44130600	Weak transcription	Monocytes-CD14+_RO01746	blood
5	chr18:44126600-44130800	Weak transcription	Spleen	Spleen
6	chr18:44126600-44131200	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr18:44126600-44132200	Weak transcription	Rectal Smooth Muscle	rectum
8	chr18:44126600-44133800	Weak transcription	Brain Hippocampus Middle	brain
9	chr18:44126600-44133800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr18:44126600-44134000	Weak transcription	Brain Angular Gyrus	brain
11	chr18:44126600-44135000	Weak transcription	Brain Cingulate Gyrus	brain
12	chr18:44126600-44137200	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr18:44126600-44139200	Weak transcription	Lung	lung
14	chr18:44126600-44143000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr18:44128000-44129600	Enhancers	Stomach Smooth Muscle	stomach
16	chr18:44128200-44129200	Enhancers	Duodenum Smooth Muscle	Duodenum
17	chr18:44128200-44130200	Enhancers	Fetal Stomach	stomach

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Input of quick search could be:

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

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