Variant report

Variant	rs401454
Chromosome Location	chr7:137998678-137998679
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	chr7:137926916..137928434-chr7:137998152..138000341,2	K562	blood:
2	chr7:137995053..137999099-chr7:138144129..138146392,3	K562	blood:

Variant related genes	Relation type
ENSG00000122779	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1035329	0.80[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11536612	0.92[ASN][1000 genomes]
rs12707380	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1691717	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs357374	0.83[ASN][1000 genomes]
rs357375	0.83[ASN][1000 genomes]
rs357380	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs357387	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs357413	0.83[EUR][1000 genomes]
rs357415	0.87[EUR][1000 genomes]
rs357416	0.87[EUR][1000 genomes]
rs357417	0.88[EUR][1000 genomes]
rs357419	0.91[EUR][1000 genomes]
rs357420	0.88[EUR][1000 genomes]
rs357434	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs357436	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs357439	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs357441	0.82[EUR][1000 genomes]
rs357443	0.83[EUR][1000 genomes]
rs357444	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs357452	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs357453	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs368043	0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs368370	0.87[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs373089	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs376305	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs386059	0.98[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs396783	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs402615	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs403675	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs407702	0.83[ASN][1000 genomes]
rs409365	0.97[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs410156	0.92[ASN][1000 genomes]
rs410187	0.90[ASN][1000 genomes]
rs414919	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs424197	0.90[ASN][1000 genomes]
rs424335	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs424847	0.90[ASN][1000 genomes]
rs443184	0.83[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	esv34048	chr7:137724092-138213119	Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv831152	chr7:137884311-138033117	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv1029101	chr7:137952620-138005671	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv5967	chr7:137988239-138015844	Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv499698	chr7:137991842-138004097	Genic enhancers Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	esv1830022	chr7:137995522-137998746	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:137988600-137999200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:137995200-138012000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:137998000-138000200	Enhancers	K562	blood
4	chr7:137998000-138000400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr7:137998200-137999800	Enhancers	Stomach Mucosa	stomach
6	chr7:137998600-137999400	Enhancers	Fetal Intestine Small	intestine
7	chr7:137998600-137999400	Enhancers	Sigmoid Colon	Sigmoid Colon
8	chr7:137998600-137999600	Enhancers	Placenta	Placenta
9	chr7:137998600-138001600	Enhancers	HepG2	liver
10	chr7:137998600-138002400	Enhancers	Fetal Intestine Large	intestine

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