Variant report

Variant	rs7387683
Chromosome Location	chr8:8923060-8923061
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:8895456..8895966-chr8:8922957..8923902,2	MCF-7	breast:
2	chr8:8922931..8923921-chr8:9007807..9008747,13	K562	blood:
3	chr8:8922824..8923700-chr8:9130087..9130667,2	MCF-7	breast:
4	chr8:8922951..8924047-chr8:9007863..9008877,16	MCF-7	breast:
5	chr8:8922930..8923887-chr8:9195546..9196445,3	K562	blood:
6	chr8:8922328..8927101-chr8:9005412..9009075,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000173281	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1016512	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1045528	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10503395	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13249731	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13250674	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs13250919	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs13258661	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13260103	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13261370	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13263480	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13273769	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs13273871	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13274157	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13276286	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs13276537	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13281029	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1430931	0.80[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs17155162	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2044389	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28393746	0.85[EUR][1000 genomes]
rs34111588	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs34391124	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34412730	0.84[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34418902	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34712023	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34752993	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs34854114	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs35227233	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs35616716	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs35808561	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs3958881	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4841088	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4841092	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs55634245	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55696609	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs66483157	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs66869483	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs67139167	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs67259528	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs67434672	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs67575865	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs67958495	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs68043139	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs6985908	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6989707	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6990134	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6993811	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6994214	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6994551	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7008080	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7012302	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs71514525	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs71514527	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73195799	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs73197711	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73197712	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7816149	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7816450	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9650628	0.80[AMR][1000 genomes];0.81[EUR][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	nsv890331	chr8:8093240-8971100	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats 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 miRNA target site	43 gene(s)	inside rSNPs	diseases
2	nsv917117	chr8:8621658-9313799	Active TSS Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv831229	chr8:8751523-8926235	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
4	nsv1022468	chr8:8857853-9209167	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv539460	chr8:8857853-9209167	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv817373	chr8:8857854-9361049	Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:8915000-8923600	Weak transcription	Duodenum Mucosa	Duodenum
2	chr8:8915400-8928000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr8:8916000-8923200	Weak transcription	Skeletal Muscle Female	skeletal muscle
4	chr8:8916000-8923400	Weak transcription	Osteobl	bone
5	chr8:8916000-8935200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr8:8916200-8923400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr8:8916600-8923400	Weak transcription	Fetal Heart	heart
8	chr8:8918800-8923600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr8:8919200-8923400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr8:8920400-8923400	Weak transcription	Fetal Intestine Small	intestine
11	chr8:8920400-8923400	Weak transcription	Stomach Mucosa	stomach
12	chr8:8921600-8924000	Enhancers	K562	blood
13	chr8:8921800-8923600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr8:8922400-8923600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr8:8922400-8923600	Weak transcription	Fetal Intestine Large	intestine
16	chr8:8922800-8923400	Enhancers	Primary neutrophils fromperipheralblood	blood
17	chr8:8922800-8923400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr8:8922800-8924600	Enhancers	Primary B cells from peripheral blood	blood
19	chr8:8923000-8923800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr8:8923000-8924200	Enhancers	Primary monocytes fromperipheralblood	blood

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