Variant report

Variant	rs55795881
Chromosome Location	chr7:78379381-78379382
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10485911	0.81[EUR][1000 genomes]
rs1496767	0.88[EUR][1000 genomes]
rs16886265	0.84[EUR][1000 genomes]
rs16886302	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17383882	0.88[EUR][1000 genomes]
rs17450926	0.80[AFR][1000 genomes]
rs35696843	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55917954	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs56364307	0.89[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs60460465	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73702968	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	nsv1019355	chr7:78319575-78399845	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv607657	chr7:78329795-78483211	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78363600-78380400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:78372400-78391600	Weak transcription	Pancreas	Pancrea
3	chr7:78372400-78395200	Weak transcription	Aorta	Aorta
4	chr7:78374800-78379800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr7:78375800-78381000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr7:78376000-78380600	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr7:78376000-78384600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:78377200-78381000	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr7:78377200-78384000	Weak transcription	Psoas Muscle	Psoas
10	chr7:78377200-78385400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr7:78377400-78380600	Weak transcription	Brain Anterior Caudate	brain
12	chr7:78378000-78381000	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr7:78378400-78380000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr7:78378600-78379800	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr7:78378800-78379800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr7:78378800-78380200	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr7:78378800-78381200	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr7:78379000-78380400	Weak transcription	Brain Substantia Nigra	brain
19	chr7:78379000-78380800	Weak transcription	Brain Angular Gyrus	brain
20	chr7:78379000-78380800	Weak transcription	Brain Hippocampus Middle	brain
21	chr7:78379000-78381000	Weak transcription	Brain Cingulate Gyrus	brain
22	chr7:78379200-78379600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr7:78379200-78380200	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr7:78379200-78382800	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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