Variant report

Variant	rs72731111
Chromosome Location	chr15:49908907-49908908
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	GATA3	chr15:49908724-49909620	MCF-7	breast:	n/a	chr15:49909220-49909228

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:49908390..49910883-chr15:49911944..49913811,3	MCF-7	breast:

Variant related genes	Relation type
DTWD1	TF binding region
FAM227B	TF binding region
ENSG00000104047	Chromatin interaction
ENSG00000166262	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs12591533	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12594585	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12595447	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17482833	0.87[ASN][1000 genomes]
rs34833569	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57496745	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs58275754	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs59589271	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72729121	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72729125	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72729127	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72729130	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72729132	0.93[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72729174	0.86[EUR][1000 genomes]
rs72729189	0.86[EUR][1000 genomes]
rs72729199	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72731108	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72731116	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72731119	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs72731121	0.88[EUR][1000 genomes]
rs72731122	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72731124	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs72731125	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72731137	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72731140	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv569392	chr15:49789413-49926300	ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
2	nsv431388	chr15:49835663-49997483	Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:49895600-49911400	Weak transcription	Psoas Muscle	Psoas
2	chr15:49896000-49912200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr15:49896600-49912000	Weak transcription	Brain Cingulate Gyrus	brain
4	chr15:49896800-49912000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr15:49897000-49911400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr15:49897800-49911800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr15:49898000-49911600	Weak transcription	Brain Substantia Nigra	brain
8	chr15:49898200-49911400	Weak transcription	Pancreas	Pancrea
9	chr15:49898200-49911800	Weak transcription	Fetal Intestine Large	intestine
10	chr15:49898200-49912200	Weak transcription	Fetal Stomach	stomach
11	chr15:49898200-49912800	Weak transcription	Esophagus	oesophagus
12	chr15:49898400-49911600	Weak transcription	Brain Hippocampus Middle	brain
13	chr15:49898400-49912000	Weak transcription	Right Ventricle	heart
14	chr15:49899000-49912000	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr15:49899800-49910800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr15:49904600-49909400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr15:49905000-49912000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr15:49905400-49912000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr15:49906000-49911600	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr15:49906800-49911600	Weak transcription	Brain Anterior Caudate	brain
21	chr15:49907200-49912000	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr15:49907400-49910000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr15:49907400-49911200	Weak transcription	Duodenum Smooth Muscle	Duodenum
24	chr15:49907400-49911600	Weak transcription	Colon Smooth Muscle	Colon
25	chr15:49907400-49911800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
26	chr15:49907400-49911800	Weak transcription	Fetal Lung	lung
27	chr15:49907400-49912000	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr15:49907400-49912200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr15:49907400-49912200	Weak transcription	HSMMtube	muscle
30	chr15:49907600-49912000	Weak transcription	HSMM	muscle
31	chr15:49907600-49912200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr15:49907600-49912200	Weak transcription	Fetal Intestine Small	intestine
33	chr15:49907600-49912200	Weak transcription	Thymus	Thymus
34	chr15:49907800-49911600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr15:49907800-49911800	Weak transcription	Primary T cells from cord blood	blood
36	chr15:49907800-49912200	Weak transcription	Liver	Liver
37	chr15:49908600-49909000	ZNF genes & repeats	Primary B cells from cord blood	blood
38	chr15:49908800-49909800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr15:49908800-49911400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr15:49908800-49912200	Weak transcription	Fetal Muscle Leg	muscle

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