Variant report

Variant	rs73365594
Chromosome Location	chr7:39226539-39226540
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:10)

rs_ID	r²[population]
rs17171541	0.93[AFR][1000 genomes]
rs17171542	0.93[AFR][1000 genomes]
rs73365515	0.93[AFR][1000 genomes]
rs73365534	0.93[AFR][1000 genomes]
rs73365575	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73367204	1.00[AMR][1000 genomes]
rs73367211	1.00[AMR][1000 genomes]
rs73367217	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73380919	1.00[AMR][1000 genomes]
rs73380927	1.00[AMR][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	nsv1024142	chr7:38978728-39300444	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv830968	chr7:39127531-39283543	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv428163	chr7:39127531-39283543	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	nsv1015572	chr7:39185895-39413053	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
5	nsv538821	chr7:39185895-39413053	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:39215000-39247000	Weak transcription	Pancreas	Pancrea
2	chr7:39225800-39226800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr7:39225800-39227000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr7:39225800-39227000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr7:39225800-39227000	Enhancers	iPS-15b Cell Line	embryonic stem cell
6	chr7:39225800-39227000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr7:39225800-39227200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:39225800-39227200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr7:39226000-39226800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
10	chr7:39226000-39227000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr7:39226000-39227200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr7:39226200-39226600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr7:39226200-39226600	Enhancers	Thymus	Thymus
14	chr7:39226200-39227200	Enhancers	H1 Cell Line	embryonic stem cell
15	chr7:39226200-39227200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr7:39226400-39227200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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