Variant report

Variant	rs61245105
Chromosome Location	chr1:217079849-217079850
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs1030849	0.84[EUR][1000 genomes]
rs12563547	0.91[EUR][1000 genomes]
rs12568315	0.81[ASN][1000 genomes]
rs1436879	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1436881	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs1436882	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1898312	0.81[EUR][1000 genomes]
rs60647584	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs61325680	0.91[EUR][1000 genomes]
rs956977	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	nsv873179	chr1:217056893-217112871	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv873180	chr1:217073060-217112871	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217062800-217087800	Weak transcription	Fetal Muscle Leg	muscle
2	chr1:217072200-217082800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr1:217074400-217080000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr1:217076800-217083600	Weak transcription	Brain Anterior Caudate	brain
5	chr1:217077000-217081600	Weak transcription	Gastric	stomach
6	chr1:217077000-217082400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:217077400-217080000	Enhancers	HMEC	breast
8	chr1:217078600-217080000	Enhancers	Duodenum Mucosa	Duodenum
9	chr1:217078600-217080000	Enhancers	Fetal Intestine Small	intestine
10	chr1:217078600-217088000	Weak transcription	Right Atrium	heart
11	chr1:217078800-217081600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr1:217079000-217086400	Weak transcription	Fetal Heart	heart
13	chr1:217079400-217081800	Weak transcription	Fetal Intestine Large	intestine
14	chr1:217079800-217080000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:217079800-217080000	Enhancers	Pancreas	Pancrea
16	chr1:217079800-217080600	Enhancers	Small Intestine	intestine

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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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