Variant report

Variant	rs4943605
Chromosome Location	chr13:39400169-39400170
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs4381466	0.84[YRI][hapmap]
rs4445773	0.82[EUR][1000 genomes]
rs4471556	0.84[EUR][1000 genomes]
rs4587834	0.84[YRI][hapmap]
rs9548459	0.81[EUR][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:15 , 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	chr13:39393600-39400400	Weak transcription	Pancreas	Pancrea
4	chr13:39394600-39423000	Weak transcription	Fetal Kidney	kidney
5	chr13:39396400-39400200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr13:39396400-39400400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr13:39397800-39400400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr13:39399000-39400400	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr13:39399000-39400400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr13:39399600-39400400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr13:39399600-39401000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr13:39399800-39400400	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr13:39399800-39400800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:39399800-39402600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr13:39400000-39400200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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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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