Variant report

Variant	rs7983965
Chromosome Location	chr13:39398416-39398417
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:13)

rs_ID	r²[population]
rs3884530	0.99[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7325406	1.00[EUR][1000 genomes]
rs7327183	1.00[EUR][1000 genomes]
rs7328965	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7335056	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7982333	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7982933	1.00[EUR][1000 genomes]
rs7983560	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9594296	0.89[AFR][1000 genomes];1.00[EUR][1000 genomes]
rs9603431	0.85[AFR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9603432	0.99[AFR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9603434	1.00[EUR][1000 genomes]
rs9805487	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832585	chr13:39233307-39424375	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	esv2754118	chr13:39347702-40222644	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 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	chr13:39389200-39404800	Weak transcription	Gastric	stomach
2	chr13:39389400-39423000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr13:39393600-39398800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr13:39393600-39400400	Weak transcription	Pancreas	Pancrea
5	chr13:39394600-39423000	Weak transcription	Fetal Kidney	kidney
6	chr13:39396000-39399600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:39396400-39399600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:39396400-39399800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr13:39396400-39400200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr13:39396400-39400400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
11	chr13:39396800-39398600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr13:39396800-39399200	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr13:39396800-39399600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr13:39397200-39399000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr13:39397200-39399400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr13:39397600-39398600	Weak transcription	HMEC	breast
17	chr13:39397800-39400400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr13:39398400-39399000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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

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