Variant report

Variant	rs6959323
Chromosome Location	chr7:137001507-137001508
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10238974	1.00[EUR][1000 genomes]
rs11983998	1.00[EUR][1000 genomes]
rs1534460	1.00[EUR][1000 genomes]
rs3898947	1.00[EUR][1000 genomes]
rs56701854	1.00[EUR][1000 genomes]
rs58274406	1.00[EUR][1000 genomes]
rs61018676	1.00[EUR][1000 genomes]
rs6961173	1.00[EUR][1000 genomes]
rs6971858	1.00[EUR][1000 genomes]
rs73450894	1.00[EUR][1000 genomes]
rs73452984	1.00[EUR][1000 genomes]
rs73452985	1.00[EUR][1000 genomes]
rs73452996	1.00[EUR][1000 genomes]
rs73455103	1.00[EUR][1000 genomes]
rs73455105	1.00[EUR][1000 genomes]
rs73728688	1.00[EUR][1000 genomes]
rs73728690	1.00[EUR][1000 genomes]
rs73728699	1.00[EUR][1000 genomes]
rs73730628	1.00[EUR][1000 genomes]
rs7800546	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029192	chr7:136433278-137147566	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv831149	chr7:136831665-137006468	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv889240	chr7:136972027-137038092	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
4	nsv889241	chr7:136976713-137038092	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv869820	chr7:136990386-137347718	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136982800-137008400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr7:136991600-137013000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr7:136993200-137007000	Genic enhancers	Cortex derived primary cultured neurospheres	brain
4	chr7:136996000-137002800	Enhancers	Brain Hippocampus Middle	brain
5	chr7:136998200-137010200	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr7:136998200-137013000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr7:136998600-137005600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr7:136999600-137002000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr7:137000000-137002800	Enhancers	Brain Cingulate Gyrus	brain
10	chr7:137000200-137002000	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr7:137000600-137004800	Weak transcription	Brain Anterior Caudate	brain
12	chr7:137000800-137001600	Enhancers	Fetal Heart	heart
13	chr7:137001000-137003800	Enhancers	Brain Angular Gyrus	brain
14	chr7:137001200-137002000	Genic enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:137001200-137002000	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr7:137001200-137002000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr7:137001200-137002200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr7:137001400-137001800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr7:137001400-137001800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr7:137001400-137001800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
21	chr7:137001400-137001800	Enhancers	Fetal Brain Male	brain
22	chr7:137001400-137002000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
23	chr7:137001400-137002000	Strong transcription	Fetal Stomach	stomach
24	chr7:137001400-137002600	Enhancers	Fetal Brain Female	brain
25	chr7:137001400-137002800	Enhancers	Brain Substantia Nigra	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links