Variant report

Variant	rs61255541
Chromosome Location	chr1:169064516-169064517
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:169064466..169066505-chr1:169069243..169071923,2	MCF-7	breast:
2	chr1:169057319..169059341-chr1:169064126..169065686,2	K562	blood:
3	chr1:169057841..169060357-chr1:169064186..169066001,2	K562	blood:
4	chr1:169053133..169065213-chr1:169070028..169077898,15	MCF-7	breast:

Variant related genes	Relation type
ENSG00000237707	Chromatin interaction
ENSG00000143153	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs16861916	0.87[AMR][1000 genomes]
rs58330569	0.82[AFR][1000 genomes]
rs61204485	1.00[AMR][1000 genomes]
rs73033742	1.00[AMR][1000 genomes]
rs73033743	1.00[AMR][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	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	esv3522071	chr1:168978325-169339044	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	esv3522072	chr1:168978325-169339044	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3' Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv831858	chr1:169022383-169179068	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	esv10418	chr1:169059628-169621268	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 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	chr1:169058800-169064600	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr1:169060400-169068000	Weak transcription	Fetal Heart	heart
3	chr1:169061200-169064600	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr1:169061400-169064600	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chr1:169062200-169065000	Weak transcription	Brain Anterior Caudate	brain
6	chr1:169062200-169067600	Weak transcription	Brain Angular Gyrus	brain
7	chr1:169062800-169064600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr1:169063400-169065000	Enhancers	HMEC	breast
9	chr1:169063800-169065200	Enhancers	Brain Hippocampus Middle	brain
10	chr1:169064000-169064600	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr1:169064000-169064800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr1:169064000-169064800	Enhancers	Rectal Mucosa Donor 29	rectum
13	chr1:169064000-169065000	Enhancers	NHEK	skin
14	chr1:169064000-169065400	Enhancers	Brain Substantia Nigra	brain
15	chr1:169064200-169064600	Weak transcription	Small Intestine	intestine
16	chr1:169064200-169064800	Enhancers	Duodenum Mucosa	Duodenum
17	chr1:169064200-169064800	Enhancers	Stomach Mucosa	stomach
18	chr1:169064200-169064800	Enhancers	HepG2	liver
19	chr1:169064400-169064800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:169064400-169064800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
21	chr1:169064400-169064800	Enhancers	Psoas Muscle	Psoas
22	chr1:169064400-169065200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:169064400-169065200	Enhancers	Brain Inferior Temporal Lobe	brain

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