Variant report

Variant	rs7523862
Chromosome Location	chr1:114443419-114443420
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:114439933..114443921-chr1:114470851..114474658,5	K562	blood:

Variant related genes	Relation type
ENSG00000235527	Chromatin interaction
ENSG00000163349	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10745340	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10776775	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10858022	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10858023	1.00[AFR][1000 genomes];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11102701	0.81[AFR][1000 genomes]
rs11582409	0.85[YRI][hapmap]
rs11584821	0.85[YRI][hapmap]
rs1217382	0.87[YRI][hapmap]
rs1217391	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap]
rs1217392	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17464525	1.00[YRI][hapmap]
rs17510162	0.85[YRI][hapmap]
rs3765598	0.85[YRI][hapmap]
rs3789613	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3811021	0.85[YRI][hapmap]
rs3827733	0.85[YRI][hapmap]
rs6661817	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6700802	0.85[YRI][hapmap]
rs7524200	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[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	esv2752424	chr1:114189958-114712958	Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	esv1826178	chr1:114331645-114471583	Strong transcription Flanking Active TSS Active TSS Weak transcription Genic enhancers Enhancers ZNF genes & repeats 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	57 gene(s)	inside rSNPs	diseases
3	esv1842398	chr1:114331645-114471583	Active TSS Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
4	esv1848035	chr1:114331645-114471583	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	57 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:114415000-114447000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr1:114420200-114446400	Weak transcription	Aorta	Aorta
3	chr1:114431800-114445400	Weak transcription	Stomach Mucosa	stomach
4	chr1:114434800-114446200	Weak transcription	Fetal Heart	heart
5	chr1:114435600-114446200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr1:114435600-114446400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr1:114435800-114444400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr1:114436000-114444600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr1:114436000-114446800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:114436200-114444600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr1:114436200-114444600	Strong transcription	Stomach Smooth Muscle	stomach
12	chr1:114436200-114445200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr1:114436200-114446600	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr1:114436200-114446600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr1:114436400-114443800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr1:114436400-114444200	Strong transcription	Primary T cells fromperipheralblood	blood
17	chr1:114436400-114444600	Strong transcription	Primary T cells from cord blood	blood
18	chr1:114436400-114445000	Strong transcription	Liver	Liver
19	chr1:114436400-114445200	Strong transcription	Brain Anterior Caudate	brain
20	chr1:114436400-114445600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr1:114436600-114444600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr1:114436600-114445600	Strong transcription	Fetal Thymus	thymus
23	chr1:114436800-114443800	Strong transcription	Primary B cells from peripheral blood	blood
24	chr1:114436800-114444400	Strong transcription	Dnd41	blood
25	chr1:114436800-114445200	Strong transcription	Skeletal Muscle Female	skeletal muscle
26	chr1:114436800-114445600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr1:114436800-114445600	Strong transcription	Osteobl	bone
28	chr1:114436800-114446400	Strong transcription	Fetal Muscle Trunk	muscle
29	chr1:114437000-114444600	Strong transcription	Thymus	Thymus
30	chr1:114437000-114445600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr1:114437000-114445600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr1:114437000-114445600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr1:114437200-114444000	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr1:114437200-114444400	Strong transcription	Sigmoid Colon	Sigmoid Colon
35	chr1:114437200-114444600	Strong transcription	HUES64 Cell Line	embryonic stem cell
36	chr1:114437200-114445600	Strong transcription	Fetal Muscle Leg	muscle
37	chr1:114437400-114444200	Strong transcription	Skeletal Muscle Male	skeletal muscle
38	chr1:114437400-114444400	Strong transcription	Placenta	Placenta
39	chr1:114437400-114445200	Strong transcription	Primary hematopoietic stem cells short term culture	blood
40	chr1:114437400-114445400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr1:114437400-114445600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr1:114437600-114444600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr1:114437600-114446400	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr1:114437800-114444400	Strong transcription	Cortex derived primary cultured neurospheres	brain
45	chr1:114437800-114445400	Strong transcription	Brain Germinal Matrix	brain
46	chr1:114437800-114445400	Strong transcription	Brain Hippocampus Middle	brain
47	chr1:114437800-114445400	Strong transcription	Left Ventricle	heart
48	chr1:114438800-114445200	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr1:114439200-114446400	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr1:114439400-114444400	Strong transcription	NH-A	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links