Variant report

Variant	rs73450935
Chromosome Location	chr15:77892636-77892637
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:77890205..77893278-chr15:77923097..77926362,3	K562	blood:
2	chr15:77890507..77893828-chr15:77894009..77899298,4	MCF-7	breast:
3	chr15:77891327..77896574-chr15:77898422..77902980,9	K562	blood:
4	chr15:77866782..77869407-chr15:77890484..77892735,2	MCF-7	breast:
5	chr15:77891099..77895017-chr15:77905947..77909078,4	K562	blood:
6	chr15:77884788..77887533-chr15:77890079..77892791,3	K562	blood:

Variant related genes	Relation type
ENSG00000169783	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs58372659	0.81[AMR][1000 genomes]
rs58490956	0.81[AMR][1000 genomes]
rs59587253	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs60309400	0.81[AMR][1000 genomes]
rs60322323	0.81[AMR][1000 genomes]
rs60789552	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73450717	0.81[AMR][1000 genomes]
rs73450724	0.81[AMR][1000 genomes]
rs73450740	0.81[AMR][1000 genomes]
rs73450925	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73450926	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73450931	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs74025306	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040852	chr15:77160237-78137541	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv916323	chr15:77485765-78121259	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv833060	chr15:77816654-78035204	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
5	nsv904415	chr15:77845959-77943935	Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv904416	chr15:77845959-77967416	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv904417	chr15:77851535-77935992	Weak transcription Flanking Active TSS Genic enhancers Enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv904418	chr15:77851535-77963887	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv1036749	chr15:77884026-77912408	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77883800-77896000	Weak transcription	Brain Hippocampus Middle	brain
2	chr15:77889400-77896000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:77889800-77896400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr15:77890200-77892800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr15:77891000-77896600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:77891000-77898800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr15:77891200-77893000	Enhancers	Fetal Stomach	stomach
8	chr15:77891200-77893400	Enhancers	Fetal Heart	heart
9	chr15:77891800-77892800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr15:77892000-77892800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr15:77892000-77892800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr15:77892000-77892800	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr15:77892000-77893000	Enhancers	H1 Cell Line	embryonic stem cell
14	chr15:77892000-77893000	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr15:77892000-77893000	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr15:77892000-77893000	Enhancers	Left Ventricle	heart
17	chr15:77892000-77893200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr15:77892000-77893200	Enhancers	K562	blood
19	chr15:77892200-77892800	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr15:77892200-77893000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr15:77892200-77893000	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr15:77892200-77893000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr15:77892200-77895200	Weak transcription	Fetal Intestine Small	intestine
24	chr15:77892200-77897200	Weak transcription	Gastric	stomach
25	chr15:77892200-77897600	Weak transcription	Right Ventricle	heart
26	chr15:77892400-77892800	Enhancers	Fetal Thymus	thymus
27	chr15:77892400-77894200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr15:77892400-77896000	Weak transcription	Fetal Brain Male	brain
29	chr15:77892400-77896200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr15:77892400-77896800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr15:77892400-77896800	Weak transcription	Lung	lung
32	chr15:77892400-77897000	Weak transcription	Right Atrium	heart
33	chr15:77892600-77893000	Enhancers	H9 Cell Line	embryonic stem cell
34	chr15:77892600-77893000	Enhancers	Stomach Smooth Muscle	stomach
35	chr15:77892600-77896000	Weak transcription	Brain Substantia Nigra	brain

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