Variant report

Variant	rs7687003
Chromosome Location	chr4:15669481-15669482
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:15667185..15670762-chr4:15673659..15675755,3	K562	blood:
2	chr4:15668976..15670549-chr4:15675107..15677746,2	MCF-7	breast:
3	chr4:15652202..15654659-chr4:15668639..15670937,2	MCF-7	breast:
4	chr4:15669222..15672294-chr4:15681695..15684873,3	K562	blood:
5	chr4:15653293..15659319-chr4:15668815..15673574,11	MCF-7	breast:
6	chr4:15669176..15670885-chr4:15682529..15684654,2	MCF-7	breast:
7	chr4:15669270..15672127-chr4:15677094..15678755,2	MCF-7	breast:
8	chr4:15664444..15667043-chr4:15668246..15669921,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000118564	Chromatin interaction
ENSG00000237765	Chromatin interaction

Extended variants
information (count: 52 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10008376	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10008975	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10214	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11728084	0.86[EUR][1000 genomes]
rs12499412	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12500587	0.85[EUR][1000 genomes]
rs12500770	0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12512883	0.82[EUR][1000 genomes]
rs12644655	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12651550	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13110674	0.88[EUR][1000 genomes]
rs13120905	0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13129739	0.81[EUR][1000 genomes]
rs13147590	0.83[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1789	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35414597	0.82[EUR][1000 genomes]
rs4235379	0.89[EUR][1000 genomes]
rs4270584	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4333182	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4453929	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4470622	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4524378	0.87[EUR][1000 genomes]
rs4557256	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4616746	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4631041	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4698402	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4698404	0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4698406	0.89[EUR][1000 genomes]
rs4698407	0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4698409	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs61021642	0.85[EUR][1000 genomes]
rs6414765	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6414767	0.81[AFR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6414768	0.88[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs6449153	0.92[EUR][1000 genomes]
rs6449161	0.88[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs6850169	0.87[EUR][1000 genomes]
rs6850422	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7438356	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7662032	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7685083	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7688984	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7696127	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9997068	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3448986	chr4:14928802-15805558	Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
2	esv2757923	chr4:15444617-15749520	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	esv2759227	chr4:15444617-15749520	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv428439	chr4:15556961-15749520	Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv1012988	chr4:15597510-16091527	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
6	nsv518830	chr4:15610771-15672200	Flanking Active TSS Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv521183	chr4:15610771-15692136	Genic enhancers Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
8	esv3361772	chr4:15666732-15684418	Transcr. at gene 5' and 3' Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7687003	FBXL5	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:15657600-15681400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr4:15658000-15672200	Weak transcription	Fetal Muscle Trunk	muscle
3	chr4:15658000-15673800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:15658000-15675200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr4:15658000-15679000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr4:15658000-15681400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr4:15658200-15670600	Weak transcription	Brain Cingulate Gyrus	brain
8	chr4:15658200-15679200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr4:15658200-15679200	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr4:15658200-15682200	Weak transcription	Fetal Stomach	stomach
11	chr4:15658600-15673000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:15658600-15679000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr4:15659800-15678600	Weak transcription	K562	blood
14	chr4:15660200-15670600	Weak transcription	Fetal Lung	lung
15	chr4:15660400-15679200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr4:15661600-15678600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr4:15662400-15678800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr4:15664800-15681800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr4:15666800-15669600	Strong transcription	Thymus	Thymus
20	chr4:15666800-15670200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr4:15667000-15670600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr4:15667400-15669800	Strong transcription	GM12878-XiMat	blood
23	chr4:15667400-15670800	Strong transcription	HUES64 Cell Line	embryonic stem cell
24	chr4:15667400-15675200	Weak transcription	Fetal Intestine Large	intestine
25	chr4:15667800-15670000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
26	chr4:15667800-15673800	Weak transcription	Fetal Intestine Small	intestine
27	chr4:15668000-15669600	Strong transcription	H1 Cell Line	embryonic stem cell
28	chr4:15668000-15669600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr4:15668000-15670000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr4:15668000-15676400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:15668200-15669600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
32	chr4:15668200-15670800	Weak transcription	HSMMtube	muscle
33	chr4:15668200-15672600	Weak transcription	Placenta	Placenta
34	chr4:15668200-15678600	Weak transcription	NHLF	lung
35	chr4:15668400-15669600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:15668400-15670000	Strong transcription	HUES6 Cell Line	embryonic stem cell
37	chr4:15668400-15670200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr4:15668400-15679000	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr4:15668400-15682800	Weak transcription	Fetal Brain Male	brain
40	chr4:15668600-15670000	Strong transcription	HMEC	breast
41	chr4:15668600-15673000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr4:15668600-15677000	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr4:15668600-15678800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr4:15668600-15679000	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr4:15668600-15681400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr4:15668800-15669800	Genic enhancers	Primary monocytes fromperipheralblood	blood
47	chr4:15668800-15678600	Weak transcription	Hela-S3	cervix
48	chr4:15669000-15669600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:15669000-15669600	Enhancers	Monocytes-CD14+_RO01746	blood
50	chr4:15669000-15670200	Strong transcription	NHEK	skin

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