Variant report

Variant	rs35872305
Chromosome Location	chr1:212446322-212446323
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:212439869..212442717-chr1:212444447..212446810,3	K562	blood:
2	chr1:212441608..212446512-chr1:212456741..212460903,9	K562	blood:
3	chr1:212446148..212447711-chr1:212451138..212453205,2	K562	blood:
4	chr1:212445933..212447648-chr1:212451138..212453935,2	K562	blood:

Variant related genes	Relation type
ENSG00000066027	Chromatin interaction

Extended variants
information (count: 39 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10863960	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10863961	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11119899	0.94[ASN][1000 genomes]
rs11576437	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11579999	0.84[ASN][1000 genomes]
rs11580285	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11585215	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11589817	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12064553	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12066356	0.94[ASN][1000 genomes]
rs12096035	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12722832	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12727947	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12728266	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12730098	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12743785	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12745269	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12747025	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1493600	0.84[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1530451	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17721302	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2358448	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34212128	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34244392	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34447409	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34740542	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55814152	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6661987	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6667199	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71646153	0.82[EUR][1000 genomes]
rs7521041	0.94[ASN][1000 genomes]
rs7531219	0.94[ASN][1000 genomes]
rs968531	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs968532	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv999738	chr1:212218618-212513690	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1009376	chr1:212292357-212680320	Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv549139	chr1:212332294-212876902	Flanking Active TSS Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	114 gene(s)	inside rSNPs	diseases
4	nsv997629	chr1:212404489-212658785	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
5	nsv535286	chr1:212404489-212658785	Strong transcription Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs35872305	RP11-15I11.3	cis	Nerve Tibial	GTEx
rs35872305	RP11-15I11.3	cis	lung	GTEx
rs35872305	RP11-15I11.3	cis	Thyroid	GTEx
rs35872305	RP11-15I11.3	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:212444400-212446400	Enhancers	Primary T cells from cord blood	blood
2	chr1:212444400-212446600	Enhancers	Fetal Intestine Small	intestine
3	chr1:212444800-212446600	Enhancers	Fetal Intestine Large	intestine
4	chr1:212445000-212446400	Enhancers	Fetal Heart	heart
5	chr1:212445200-212446400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr1:212445200-212446400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr1:212445200-212446400	Enhancers	Fetal Lung	lung
8	chr1:212445200-212446600	Enhancers	Left Ventricle	heart
9	chr1:212445200-212447200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr1:212445400-212446400	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr1:212445600-212446600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr1:212445600-212446600	Enhancers	Brain Inferior Temporal Lobe	brain
13	chr1:212445800-212446400	Weak transcription	Right Atrium	heart
14	chr1:212445800-212448400	Weak transcription	Pancreas	Pancrea
15	chr1:212446000-212446400	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr1:212446000-212457000	Weak transcription	Stomach Mucosa	stomach
17	chr1:212446000-212457600	Weak transcription	Fetal Brain Female	brain
18	chr1:212446200-212454000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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