Variant report

Variant	rs3104463
Chromosome Location	chr1:77981918-77981919
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:77981334..77981921-chr1:78148898..78149513,2	K562	blood:

Variant related genes	Relation type
ENSG00000036549	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1135921	1.00[AMR][1000 genomes]
rs1353727	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17100655	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17100694	1.00[AMR][1000 genomes]
rs17100731	1.00[AMR][1000 genomes]
rs17100781	1.00[AMR][1000 genomes]
rs17100789	1.00[AMR][1000 genomes]
rs17100941	1.00[AMR][1000 genomes]
rs2047167	1.00[AMR][1000 genomes]
rs2088519	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2256679	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2291689	1.00[AMR][1000 genomes]
rs2647495	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2647513	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2803139	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2803154	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2803166	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2803167	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2803169	1.00[AMR][1000 genomes]
rs2803170	1.00[AMR][1000 genomes]
rs3104462	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs3112830	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470719	chr1:77774413-78269207	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
2	nsv546591	chr1:77774413-78269207	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv871143	chr1:77955577-78031994	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77973600-77983400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
2	chr1:77974600-77982200	Enhancers	NHDF-Ad	bronchial
3	chr1:77978800-77982000	Enhancers	Brain Inferior Temporal Lobe	brain
4	chr1:77978800-77982400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr1:77978800-77983000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr1:77979200-77983000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr1:77979200-77984000	Weak transcription	Primary T cells from cord blood	blood
8	chr1:77979400-77982000	Enhancers	Brain Angular Gyrus	brain
9	chr1:77979400-77982400	Enhancers	Fetal Muscle Leg	muscle
10	chr1:77979800-77982000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr1:77980600-77982200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr1:77980800-77982000	Enhancers	Muscle Satellite Cultured Cells	--
13	chr1:77980800-77982400	Enhancers	HSMM	muscle
14	chr1:77980800-77999400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr1:77981000-77982000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr1:77981000-77982400	Enhancers	Brain Germinal Matrix	brain
17	chr1:77981000-77983000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
18	chr1:77981200-77982400	Enhancers	Brain Substantia Nigra	brain
19	chr1:77981200-77982600	Enhancers	Brain Cingulate Gyrus	brain
20	chr1:77981400-77982000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr1:77981400-77982200	Enhancers	Brain Anterior Caudate	brain
22	chr1:77981400-77982400	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr1:77981400-77982400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr1:77981600-77982000	Enhancers	Monocytes-CD14+_RO01746	blood
25	chr1:77981600-77982200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:77981600-77984000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:77981800-77982200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr1:77981800-77984200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr1:77981800-77987200	Weak transcription	Fetal Muscle Trunk	muscle
30	chr1:77981800-77987400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr1:77981800-77987400	Weak transcription	Brain Hippocampus Middle	brain
32	chr1:77981800-77998400	Weak transcription	Osteobl	bone
33	chr1:77981800-77999200	Weak transcription	NHLF	lung
34	chr1:77981800-77999400	Weak transcription	HSMMtube	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links