Variant report

Variant	rs2025904
Chromosome Location	chr13:111183943-111183944
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs394559	0.85[AFR][1000 genomes]
rs418543	1.00[CEU][hapmap];0.84[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71419777	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9515246	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9588184	0.85[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1038914	chr13:110860219-111190104	Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
2	nsv1046423	chr13:110936104-111286607	Weak transcription Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv832720	chr13:111100235-111295993	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv1046291	chr13:111125747-111257861	Weak transcription Active TSS Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv1045143	chr13:111126822-111242791	Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
6	nsv1044234	chr13:111143053-111370580	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	216 gene(s)	inside rSNPs	diseases
7	nsv949634	chr13:111151460-111582996	Genic enhancers Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	245 gene(s)	inside rSNPs	diseases
8	nsv901010	chr13:111165390-111286592	Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers Weak transcription Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
9	nsv1053922	chr13:111167764-111330876	Flanking Active TSS Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
10	nsv1043849	chr13:111167764-111340418	Bivalent Enhancer Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
11	nsv541924	chr13:111167764-111340418	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
12	nsv1036160	chr13:111167764-111347308	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
13	nsv541925	chr13:111167764-111347308	Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
14	nsv901011	chr13:111168951-111280002	Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	23 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:111160800-111209600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr13:111167000-111190800	Weak transcription	Fetal Kidney	kidney
3	chr13:111176000-111185800	Enhancers	Stomach Mucosa	stomach
4	chr13:111178600-111188000	Weak transcription	Primary B cells from cord blood	blood
5	chr13:111180000-111187600	Weak transcription	Fetal Stomach	stomach
6	chr13:111180000-111188000	Weak transcription	Right Ventricle	heart
7	chr13:111180000-111188200	Weak transcription	Brain Anterior Caudate	brain
8	chr13:111180200-111184000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr13:111180200-111189400	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr13:111180400-111186400	Weak transcription	Stomach Smooth Muscle	stomach
11	chr13:111180400-111189600	Weak transcription	Colonic Mucosa	Colon
12	chr13:111181000-111188000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr13:111181400-111184400	Enhancers	Placenta Amnion	Placenta Amnion
14	chr13:111181400-111190800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr13:111181800-111185800	Weak transcription	Brain Hippocampus Middle	brain
16	chr13:111181800-111187800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr13:111182000-111187600	Weak transcription	Fetal Intestine Large	intestine
18	chr13:111182000-111188000	Weak transcription	Right Atrium	heart
19	chr13:111182000-111192200	Weak transcription	Fetal Heart	heart
20	chr13:111182200-111185400	Weak transcription	Ovary	ovary
21	chr13:111182200-111188000	Weak transcription	Left Ventricle	heart
22	chr13:111182200-111193400	Weak transcription	Aorta	Aorta
23	chr13:111182400-111189800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr13:111182400-111193800	Weak transcription	HepG2	liver
25	chr13:111182400-111203600	Weak transcription	Brain Substantia Nigra	brain
26	chr13:111183000-111191400	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr13:111183200-111184000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr13:111183200-111184200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr13:111183200-111184400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr13:111183200-111184400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr13:111183200-111184600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr13:111183200-111184600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr13:111183400-111184000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr13:111183400-111184000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr13:111183400-111184000	Enhancers	Lung	lung
36	chr13:111183400-111184200	Enhancers	H1 Cell Line	embryonic stem cell
37	chr13:111183400-111184200	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr13:111183400-111184200	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
39	chr13:111183400-111184200	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr13:111183400-111184600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr13:111183400-111184600	Enhancers	Pancreas	Pancrea
42	chr13:111183400-111184600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr13:111183400-111184800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr13:111183400-111184800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr13:111183400-111184800	Genic enhancers	Fetal Adrenal Gland	Adrenal Gland
46	chr13:111183400-111185800	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr13:111183400-111186600	Enhancers	Adipose Nuclei	Adipose
48	chr13:111183400-111190400	Strong transcription	Fetal Intestine Small	intestine
49	chr13:111183600-111184200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr13:111183600-111184200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links