Variant report

Variant	rs11852636
Chromosome Location	chr15:78495247-78495248
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:78487022..78489077-chr15:78494616..78496936,2	MCF-7	breast:
2	chr15:78460946..78462466-chr15:78493777..78496351,2	K562	blood:
3	chr15:78425017..78427929-chr15:78494303..78496254,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs12442037	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16969575	0.82[AMR][1000 genomes]
rs2018983	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2271901	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2304823	0.94[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs56803002	0.83[ASN][1000 genomes]
rs59184904	0.82[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs59824250	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv948437	chr15:78435527-78504662	Strong transcription Bivalent Enhancer Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS 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	15 gene(s)	inside rSNPs	diseases
3	nsv904430	chr15:78466127-78507316	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv917303	chr15:78491050-79205255	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	122 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78487600-78495400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr15:78487600-78495400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr15:78487600-78495600	Weak transcription	Right Atrium	heart
4	chr15:78488400-78497000	Weak transcription	Spleen	Spleen
5	chr15:78492800-78500200	Enhancers	Fetal Muscle Leg	muscle
6	chr15:78493200-78495400	Weak transcription	Fetal Intestine Small	intestine
7	chr15:78493200-78495400	Weak transcription	Pancreas	Pancrea
8	chr15:78493400-78495400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
9	chr15:78493400-78496000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr15:78493800-78504200	Enhancers	Brain Substantia Nigra	brain
11	chr15:78494200-78508800	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr15:78494200-78509800	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr15:78494800-78508800	Enhancers	Brain Hippocampus Middle	brain
14	chr15:78494800-78509800	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr15:78495000-78495400	Enhancers	Brain Anterior Caudate	brain
16	chr15:78495000-78500200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr15:78495000-78500400	Enhancers	Brain Angular Gyrus	brain
18	chr15:78495000-78504200	Enhancers	Brain Cingulate Gyrus	brain
19	chr15:78495200-78497400	Enhancers	Right Ventricle	heart
20	chr15:78495200-78498400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr15:78495200-78499600	Enhancers	Fetal Heart	heart

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