Variant report

Variant	rs1778213
Chromosome Location	chr1:95061054-95061055
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs11165177	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12079330	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12092812	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1343481	0.87[ASN][1000 genomes]
rs1629015	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1747649	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1747650	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1747651	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1747652	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1747653	0.99[ASN][1000 genomes]
rs1747654	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1747655	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1747657	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1747659	0.96[ASN][1000 genomes]
rs1772899	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1772900	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1772901	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1772903	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1778211	0.99[ASN][1000 genomes]
rs1778214	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1778216	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4847313	0.86[ASN][1000 genomes]
rs841709	0.96[ASN][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	nsv870696	chr1:95005220-95081587	Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv871391	chr1:95005220-95083836	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1001587	chr1:95027691-95318680	Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
4	nsv871279	chr1:95028981-95083836	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	esv1804937	chr1:95051930-95081587	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:95046000-95065400	Weak transcription	Fetal Intestine Large	intestine
2	chr1:95055000-95061400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr1:95055000-95061600	Enhancers	Brain Anterior Caudate	brain
4	chr1:95055000-95062000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
5	chr1:95055400-95061800	Enhancers	Cortex derived primary cultured neurospheres	brain
6	chr1:95056200-95067800	Weak transcription	Gastric	stomach
7	chr1:95056400-95061400	Weak transcription	Fetal Lung	lung
8	chr1:95056800-95061200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr1:95056800-95061200	Weak transcription	NHLF	lung
10	chr1:95056800-95069000	Weak transcription	Right Atrium	heart
11	chr1:95057000-95061600	Enhancers	Brain Hippocampus Middle	brain
12	chr1:95057400-95069000	Weak transcription	Aorta	Aorta
13	chr1:95057800-95061400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr1:95059000-95061400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:95059200-95061600	Weak transcription	Brain Germinal Matrix	brain
16	chr1:95059200-95062800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr1:95059400-95061200	Weak transcription	Stomach Mucosa	stomach
18	chr1:95059400-95064600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
19	chr1:95059400-95074200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr1:95059600-95061200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr1:95059800-95061200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr1:95060200-95062400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr1:95060400-95061600	Enhancers	Brain Cingulate Gyrus	brain
24	chr1:95060400-95063000	Weak transcription	Hela-S3	cervix
25	chr1:95060600-95061200	Weak transcription	Brain Substantia Nigra	brain
26	chr1:95060600-95061600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr1:95060600-95061600	Enhancers	NHEK	skin
28	chr1:95060600-95062000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr1:95060600-95062000	Enhancers	Fetal Muscle Leg	muscle
30	chr1:95060800-95061400	Weak transcription	Brain Angular Gyrus	brain
31	chr1:95060800-95061800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr1:95060800-95063400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr1:95060800-95064400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr1:95060800-95065400	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr1:95061000-95061200	Enhancers	Placenta	Placenta
36	chr1:95061000-95061800	Enhancers	Fetal Intestine Small	intestine
37	chr1:95061000-95062000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr1:95061000-95062000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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