Variant report

Variant	rs16998532
Chromosome Location	chr21:41168033-41168034
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:41161226..41165062-chr21:41165469..41170017,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000183067	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs16998436	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs16998444	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16998490	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16998519	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs16998521	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16998534	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16998550	0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16998553	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16998556	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16998576	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17753538	0.91[EUR][1000 genomes]
rs2837204	0.91[ASN][1000 genomes]
rs456303	0.93[ASN][1000 genomes]
rs55739464	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56955296	0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs67969662	0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73215346	0.89[EUR][1000 genomes]
rs73217283	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73217284	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs73217286	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73217292	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73217299	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73217300	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73219407	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73219481	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73219482	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73219485	0.91[EUR][1000 genomes]
rs73219486	0.91[EUR][1000 genomes]
rs73219489	0.91[EUR][1000 genomes]
rs73219490	0.91[EUR][1000 genomes]
rs73219491	0.91[EUR][1000 genomes]
rs73221250	0.89[EUR][1000 genomes]
rs73904413	0.89[ASN][1000 genomes]
rs73904418	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73904443	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8127368	0.87[EUR][1000 genomes];0.92[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	nsv1061454	chr21:40757973-41265404	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats 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	33 gene(s)	inside rSNPs	diseases
2	nsv1057956	chr21:40907707-41393396	Enhancers Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv544444	chr21:40907707-41393396	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv1065086	chr21:41034806-41429078	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv544445	chr21:41034806-41429078	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv834099	chr21:41076873-41206030	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:41161000-41171000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr21:41161400-41170400	Weak transcription	Right Atrium	heart
3	chr21:41161400-41180000	Weak transcription	Pancreas	Pancrea
4	chr21:41162600-41170200	Weak transcription	Left Ventricle	heart
5	chr21:41163600-41170400	Weak transcription	Fetal Heart	heart
6	chr21:41164200-41185600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr21:41165800-41168200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr21:41166000-41168600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr21:41166200-41173200	Weak transcription	Placenta	Placenta
10	chr21:41167800-41168600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
11	chr21:41168000-41168400	Enhancers	Right Ventricle	heart
12	chr21:41168000-41169000	Enhancers	Fetal Muscle Leg	muscle

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