Variant report

Variant	rs12698832
Chromosome Location	chr7:69464184-69464185
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:69453365..69456606-chr7:69459884..69464599,5	K562	blood:
2	chr7:69459148..69462116-chr7:69464154..69466270,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12698809	0.83[ASN][1000 genomes]
rs12698810	0.83[ASN][1000 genomes]
rs12698811	0.81[ASN][1000 genomes]
rs12698818	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12698821	0.88[ASN][1000 genomes]
rs12698823	0.82[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs12698824	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12698827	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12698828	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12698829	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12698831	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12698833	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12698854	0.85[ASN][1000 genomes]
rs12698857	0.85[CEU][hapmap]
rs12698860	0.85[ASN][1000 genomes]
rs12698863	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13221186	0.88[ASN][1000 genomes]
rs13221694	0.87[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13224557	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13227197	0.85[ASN][1000 genomes]
rs13228686	0.90[ASN][1000 genomes]
rs13229256	0.85[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13238398	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34215431	0.83[EUR][1000 genomes]
rs71535673	0.85[ASN][1000 genomes]
rs71535674	0.83[ASN][1000 genomes]
rs7785360	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7788868	0.85[ASN][1000 genomes]
rs7789364	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021538	chr7:69130236-69575753	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv538917	chr7:69130236-69575753	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv817276	chr7:69130237-69736834	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1018749	chr7:69149029-69995112	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv492242	chr7:69330737-69520566	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1018289	chr7:69383450-69650885	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv538922	chr7:69383450-69650885	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv532782	chr7:69383651-70189959	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1034281	chr7:69403828-69548378	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv538923	chr7:69403828-69548378	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1034182	chr7:69406172-69529294	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv538924	chr7:69406172-69529294	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	esv2758119	chr7:69412504-69594161	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	esv2759536	chr7:69412504-69594161	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv607429	chr7:69430748-69553093	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv1028705	chr7:69453983-69524628	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:69455800-69470400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr7:69459200-69464800	Weak transcription	Fetal Thymus	thymus
3	chr7:69460200-69470200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr7:69460200-69471600	Weak transcription	Fetal Intestine Small	intestine
5	chr7:69461400-69465200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr7:69461400-69465800	Weak transcription	Brain Hippocampus Middle	brain
7	chr7:69461400-69466200	Weak transcription	Brain Substantia Nigra	brain
8	chr7:69461400-69471000	Weak transcription	Right Atrium	heart
9	chr7:69461400-69471400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:69461400-69471600	Weak transcription	Right Ventricle	heart
11	chr7:69461600-69465800	Weak transcription	Cortex derived primary cultured neurospheres	brain
12	chr7:69461600-69465800	Weak transcription	Left Ventricle	heart
13	chr7:69461600-69466000	Weak transcription	Brain Germinal Matrix	brain
14	chr7:69461600-69474000	Weak transcription	Psoas Muscle	Psoas
15	chr7:69462200-69470200	Weak transcription	Colon Smooth Muscle	Colon
16	chr7:69462800-69465200	Weak transcription	Fetal Brain Female	brain
17	chr7:69463000-69465000	Weak transcription	Fetal Brain Male	brain
18	chr7:69463200-69470000	Weak transcription	Fetal Stomach	stomach
19	chr7:69463400-69466000	Weak transcription	Stomach Smooth Muscle	stomach
20	chr7:69463800-69464400	Enhancers	Ovary	ovary
21	chr7:69464000-69465200	Enhancers	Fetal Heart	heart

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