Variant report

Variant	rs10153708
Chromosome Location	chr2:187450542-187450543
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:187359427..187362374-chr2:187449290..187451810,2	K562	blood:
2	chr2:187442776..187446488-chr2:187447901..187451766,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000213953	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10191572	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10191888	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10196722	0.83[AMR][1000 genomes]
rs10202802	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13386665	0.83[AMR][1000 genomes]
rs13396060	0.83[AMR][1000 genomes]
rs13403385	0.83[AMR][1000 genomes]
rs13405296	0.83[AMR][1000 genomes]
rs13410314	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs13419307	1.00[ASW][hapmap];1.00[LWK][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16828044	0.83[AMR][1000 genomes]
rs16828048	0.83[AMR][1000 genomes]
rs16828049	0.83[AMR][1000 genomes]
rs56316122	0.83[AMR][1000 genomes]
rs56385600	1.00[AMR][1000 genomes]
rs59828675	0.83[AMR][1000 genomes]
rs6746367	0.83[AMR][1000 genomes]
rs6758885	0.83[AMR][1000 genomes]
rs73044325	0.83[AMR][1000 genomes]
rs73044336	0.83[AMR][1000 genomes]
rs73044342	0.83[AMR][1000 genomes]
rs73979316	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73981329	0.83[AMR][1000 genomes]
rs73981332	0.83[AMR][1000 genomes]
rs73981336	1.00[AMR][1000 genomes]
rs9973506	0.83[AMR][1000 genomes]
rs9973742	0.83[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757844	chr2:187332780-187580547	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv2759107	chr2:187332780-187580547	Enhancers Bivalent/Poised TSS Active TSS Genic enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv1004309	chr2:187389880-187455946	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv536082	chr2:187389880-187455946	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv875552	chr2:187393729-187505486	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv1014203	chr2:187413781-187477586	Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
7	nsv536083	chr2:187413781-187477586	Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
8	esv2756507	chr2:187416494-187470494	Flanking Active TSS Bivalent/Poised TSS Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
9	esv2756956	chr2:187416599-187492742	Enhancers Flanking Active TSS Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
10	nsv818105	chr2:187423298-187481835	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
11	esv2753217	chr2:187424494-187470494	Flanking Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:187435600-187453800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr2:187441400-187453400	Weak transcription	NHEK	skin
3	chr2:187441800-187453600	Weak transcription	Brain Substantia Nigra	brain
4	chr2:187442400-187453800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr2:187443000-187453400	Weak transcription	A549	lung
6	chr2:187445800-187454200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr2:187448400-187453400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr2:187448600-187451600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr2:187449200-187451400	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr2:187449800-187451200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr2:187449800-187452000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr2:187450000-187451400	Enhancers	Fetal Intestine Small	intestine
13	chr2:187450200-187450600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr2:187450200-187450600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr2:187450200-187450800	Enhancers	Fetal Intestine Large	intestine
16	chr2:187450200-187451200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr2:187450400-187450800	Enhancers	Adipose Nuclei	Adipose
18	chr2:187450400-187451200	Enhancers	HUES6 Cell Line	embryonic stem cell

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