Variant report

Variant	rs7546997
Chromosome Location	chr1:77560463-77560464
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1098123	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs1098127	0.86[AFR][1000 genomes]
rs1779167	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs2653468	1.00[YRI][hapmap];0.84[AFR][1000 genomes]
rs2653470	1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs2799569	0.86[AFR][1000 genomes]
rs58815389	1.00[AFR][1000 genomes]
rs61484997	0.94[AFR][1000 genomes]
rs74090599	0.87[AFR][1000 genomes]
rs74090600	1.00[AFR][1000 genomes]
rs74092420	0.83[AFR][1000 genomes]
rs839806	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs839811	1.00[YRI][hapmap]
rs839812	0.82[YRI][hapmap]
rs839817	0.82[AFR][1000 genomes]
rs839819	1.00[YRI][hapmap];0.86[AFR][1000 genomes]
rs839833	0.82[YRI][hapmap]
rs839837	1.00[YRI][hapmap];0.88[AFR][1000 genomes]
rs839839	0.92[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003826	chr1:76965331-77656929	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	nsv535006	chr1:76965331-77656929	Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv830292	chr1:77425571-77584307	Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77547800-77564600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr1:77547800-77570600	Weak transcription	Ovary	ovary
3	chr1:77548400-77570400	Weak transcription	Left Ventricle	heart
4	chr1:77550400-77570400	Weak transcription	Aorta	Aorta
5	chr1:77553000-77560600	Weak transcription	Primary B cells from cord blood	blood
6	chr1:77553800-77562000	Weak transcription	Primary T cells from cord blood	blood
7	chr1:77555000-77577800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:77555400-77565800	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr1:77556000-77560800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr1:77556000-77614400	Weak transcription	Primary T cells fromperipheralblood	blood
11	chr1:77556200-77560800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr1:77556400-77560800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:77556400-77560800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr1:77558600-77569000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr1:77560200-77561600	Enhancers	Pancreatic Islets	Pancreatic Islet
16	chr1:77560400-77560600	Enhancers	Fetal Muscle Leg	muscle

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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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