Variant report

Variant	rs248705
Chromosome Location	chr5:126994381-126994382
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	chr5:126992498..126994674-chr5:126998556..127000281,2	K562	blood:

Variant related genes	Relation type
ENSG00000248799	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10072627	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1086482	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1123820	0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs13182486	0.96[CEU][hapmap]
rs2138273	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs248693	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs248694	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.84[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs248695	0.81[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs248697	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs248699	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs248704	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs248707	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs248708	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs248714	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs248719	0.84[ASN][1000 genomes]
rs248723	0.88[ASN][1000 genomes]
rs248725	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs248727	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs248728	0.81[ASN][1000 genomes]
rs248729	0.81[ASN][1000 genomes]
rs248734	0.82[ASN][1000 genomes]
rs2569143	0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2673751	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2673762	0.84[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs790835	0.81[ASN][1000 genomes]
rs790837	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][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	nsv1033607	chr5:126385181-127304459	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv830479	chr5:126849254-127053121	Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv1021483	chr5:126927834-127304873	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv830480	chr5:126964751-127124522	Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv599664	chr5:126974071-127016256	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:126988000-126996000	Weak transcription	Rectal Smooth Muscle	rectum
2	chr5:126991400-126995800	Weak transcription	Fetal Stomach	stomach
3	chr5:126991400-127001800	Weak transcription	Fetal Lung	lung
4	chr5:126992600-126995200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr5:126992600-126995600	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr5:126992600-126995600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr5:126992600-126995600	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr5:126992800-126995400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr5:126992800-126995400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
10	chr5:126992800-126995600	Weak transcription	Fetal Muscle Leg	muscle
11	chr5:126993400-126995400	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr5:126993400-126995600	Weak transcription	Psoas Muscle	Psoas
13	chr5:126993600-126995400	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr5:126994200-126994800	Enhancers	Colon Smooth Muscle	Colon

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