Variant report

Variant	rs56701854
Chromosome Location	chr7:137008349-137008350
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10238974	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10256297	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs11983998	1.00[EUR][1000 genomes]
rs1534460	1.00[EUR][1000 genomes]
rs3898947	1.00[EUR][1000 genomes]
rs58274406	1.00[EUR][1000 genomes]
rs58644717	0.84[ASN][1000 genomes]
rs61018676	1.00[EUR][1000 genomes]
rs6959323	1.00[EUR][1000 genomes]
rs6961173	1.00[EUR][1000 genomes]
rs6971858	1.00[EUR][1000 genomes]
rs73450894	1.00[EUR][1000 genomes]
rs73452984	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs73452985	0.84[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.84[ASN][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:7 , 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	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
3	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
4	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
5	nsv1027868	chr7:137004690-137311653	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv539134	chr7:137004690-137311653	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv889242	chr7:137005808-137081223	Bivalent/Poised TSS Flanking Active TSS Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 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	chr7:136998200-137010200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr7:136998200-137013000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:137001800-137016200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr7:137002000-137010400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:137002000-137013000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr7:137002000-137020000	Weak transcription	Fetal Stomach	stomach
9	chr7:137002200-137010000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr7:137002800-137010000	Weak transcription	Brain Cingulate Gyrus	brain
11	chr7:137003800-137009800	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr7:137004600-137009600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr7:137004800-137016200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr7:137006000-137009000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr7:137006000-137009400	Weak transcription	Brain Substantia Nigra	brain
16	chr7:137006000-137010400	Weak transcription	Brain Angular Gyrus	brain
17	chr7:137006000-137011200	Weak transcription	Brain Anterior Caudate	brain
18	chr7:137006800-137009000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr7:137007600-137008600	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
20	chr7:137007600-137009600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:137008000-137010000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr7:137008000-137013000	Weak transcription	NH-A	brain

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