Variant report

Variant	rs67219137
Chromosome Location	chr7:78134109-78134110
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs12670044	0.85[EUR][1000 genomes]
rs16886179	0.83[EUR][1000 genomes]
rs17150922	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3801362	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56309632	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs56332610	0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62467108	0.85[EUR][1000 genomes]
rs62467119	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467120	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62467121	0.92[AFR][1000 genomes]
rs62467122	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62468562	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62468563	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62468566	0.92[ASN][1000 genomes]
rs62468568	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs62468570	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62468573	0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs62468578	0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73141150	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022764	chr7:77911072-78316607	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78119600-78145600	Weak transcription	Ovary	ovary
2	chr7:78122600-78143800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr7:78126200-78143800	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr7:78127800-78140000	Weak transcription	Brain Hippocampus Middle	brain
5	chr7:78128200-78144000	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr7:78128200-78145800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
7	chr7:78128400-78142600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr7:78128400-78144000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr7:78128400-78144000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
10	chr7:78128600-78140200	Weak transcription	Brain Substantia Nigra	brain
11	chr7:78128600-78142600	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr7:78128600-78145800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr7:78128800-78158400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr7:78129000-78144000	Weak transcription	Pancreas	Pancrea
15	chr7:78129800-78140000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr7:78130400-78135200	Weak transcription	Aorta	Aorta
17	chr7:78130800-78139800	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr7:78131200-78144400	Weak transcription	Brain Angular Gyrus	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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