Variant report

Variant	rs10769986
Chromosome Location	chr11:9066100-9066101
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:9062855..9067296-chr11:9070515..9073195,4	K562	blood:
2	chr11:9065273..9067296-chr11:9070845..9073195,2	K562	blood:
3	chr11:9057967..9060899-chr11:9063796..9066670,2	MCF-7	breast:
4	chr11:9060449..9064388-chr11:9064769..9066551,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000175356	Chromatin interaction

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs10743099	1.00[ASN][1000 genomes]
rs1883100	0.88[ASN][1000 genomes]
rs1883101	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7125458	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3413845	chr11:8887279-9285127	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv896984	chr11:8988550-9090408	Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv33264	chr11:9007612-9311131	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
4	nsv896985	chr11:9013002-9152463	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
5	nsv467704	chr11:9059192-9125301	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
6	nsv553454	chr11:9059192-9125301	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9047200-9068600	Weak transcription	Fetal Intestine Large	intestine
2	chr11:9052400-9067800	Weak transcription	Fetal Muscle Trunk	muscle
3	chr11:9052800-9069800	Weak transcription	Gastric	stomach
4	chr11:9058400-9099800	Weak transcription	Aorta	Aorta
5	chr11:9059200-9074000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr11:9059600-9068000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr11:9060000-9068600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr11:9060400-9066400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr11:9062000-9068400	Weak transcription	Adipose Nuclei	Adipose
10	chr11:9062200-9068000	Weak transcription	Pancreas	Pancrea
11	chr11:9063600-9068000	Weak transcription	Placenta	Placenta
12	chr11:9063800-9066400	Weak transcription	Fetal Stomach	stomach
13	chr11:9063800-9067200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr11:9064400-9067800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr11:9064400-9067800	Weak transcription	Rectal Smooth Muscle	rectum
16	chr11:9064600-9068400	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr11:9064600-9069000	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr11:9064800-9069000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr11:9065600-9073400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr11:9065800-9068000	Enhancers	Stomach Smooth Muscle	stomach
21	chr11:9066000-9066400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr11:9066000-9067200	Genic enhancers	Fetal Lung	lung
23	chr11:9066000-9081800	Weak transcription	Small Intestine	intestine

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