Variant report

Variant	rs17059828
Chromosome Location	chr13:39980289-39980290
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs28394096	0.94[AFR][1000 genomes];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4142534	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.99[AFR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4943662	0.88[ASN][1000 genomes]
rs7334879	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9576786	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][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	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
2	nsv1054600	chr13:39801283-40545027	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1036674	chr13:39841482-40008117	Bivalent Enhancer Genic enhancers Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv900008	chr13:39962791-40020267	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:39972800-39988600	Weak transcription	Fetal Muscle Leg	muscle
2	chr13:39975800-39981000	Weak transcription	Right Ventricle	heart
3	chr13:39975800-39988400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr13:39975800-39988600	Weak transcription	Right Atrium	heart
5	chr13:39976000-39981000	Weak transcription	Brain Substantia Nigra	brain
6	chr13:39976200-39984000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr13:39976600-39990600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:39977000-39987800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr13:39977200-39981000	Weak transcription	Left Ventricle	heart
10	chr13:39977200-39983800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr13:39977400-39983600	Weak transcription	Brain Hippocampus Middle	brain
12	chr13:39977600-39982600	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr13:39977800-39984400	Weak transcription	Psoas Muscle	Psoas
14	chr13:39979200-39981800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr13:39979400-39980400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr13:39979400-39980400	Enhancers	Fetal Heart	heart
17	chr13:39979400-39981600	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr13:39979400-39983600	Weak transcription	Fetal Brain Male	brain
19	chr13:39979600-39980400	Enhancers	H1 Cell Line	embryonic stem cell
20	chr13:39979600-39980400	Enhancers	Brain Cingulate Gyrus	brain
21	chr13:39979600-39981600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr13:39979800-39980400	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr13:39980000-39981000	Weak transcription	Ovary	ovary
24	chr13:39980000-39983600	Weak transcription	Brain Anterior Caudate	brain
25	chr13:39980000-39983600	Weak transcription	Fetal Lung	lung
26	chr13:39980000-39983800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr13:39980000-39983800	Weak transcription	NHDF-Ad	bronchial
28	chr13:39980000-39984000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr13:39980000-39984000	Weak transcription	NHLF	lung
30	chr13:39980200-39981000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr13:39980200-39981400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr13:39980200-39982400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr13:39980200-39983200	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr13:39980200-39983200	Weak transcription	Brain Angular Gyrus	brain
35	chr13:39980200-39983600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr13:39980200-39983600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:39980200-39983800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr13:39980200-39984400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr13:39980200-39988600	Weak transcription	Fetal Stomach	stomach

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