Variant report

Variant	rs2803143
Chromosome Location	chr1:77890022-77890023
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	chr1:77884906..77887618-chr1:77887940..77890792,2	K562	blood:

Variant related genes	Relation type
ENSG00000251767	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10518551	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10518553	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11162337	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11162338	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17100530	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17371324	0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17379910	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17380099	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2256735	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2349965	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2647514	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2647515	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2647517	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2647518	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2647519	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2647521	0.91[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2803146	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2882289	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3104461	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3112829	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4342893	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4402168	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4638175	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs59417372	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6703133	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7415865	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7417056	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1005183	chr1:77728990-77949309	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv535010	chr1:77728990-77949309	Bivalent Enhancer Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv932557	chr1:77730247-77958687	Flanking Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1003714	chr1:77756861-77949309	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	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
6	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
7	esv1848735	chr1:77885282-77918347	Weak transcription ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	nsv871605	chr1:77889505-77918347	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:33 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:77872200-77893400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr1:77872200-77913800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr1:77884400-77890400	Enhancers	Primary T helper cells fromperipheralblood	blood
4	chr1:77884800-77890600	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr1:77885400-77890600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr1:77887200-77890200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr1:77888000-77893600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr1:77888000-77897000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr1:77888200-77893400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr1:77888400-77891600	Weak transcription	Brain Anterior Caudate	brain
11	chr1:77888400-77892000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr1:77888400-77893600	Weak transcription	Brain Angular Gyrus	brain
13	chr1:77888800-77892000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr1:77889000-77890200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr1:77889000-77890400	Enhancers	HSMMtube	muscle
16	chr1:77889000-77890600	Enhancers	NHLF	lung
17	chr1:77889000-77890800	Enhancers	NHDF-Ad	bronchial
18	chr1:77889200-77890800	Enhancers	Muscle Satellite Cultured Cells	--
19	chr1:77889200-77892000	Weak transcription	Primary T cells from cord blood	blood
20	chr1:77889400-77890200	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr1:77889400-77890400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr1:77889400-77890600	Enhancers	HSMM	muscle
23	chr1:77889600-77890400	Enhancers	Osteobl	bone
24	chr1:77889600-77890600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr1:77889800-77890600	Enhancers	HMEC	breast
26	chr1:77889800-77893600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr1:77890000-77890200	Enhancers	Aorta	Aorta
28	chr1:77890000-77890200	Flanking Active TSS	Brain Hippocampus Middle	brain
29	chr1:77890000-77890400	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr1:77890000-77890400	Enhancers	HUVEC	blood vessel
31	chr1:77890000-77890600	Enhancers	Brain Substantia Nigra	brain
32	chr1:77890000-77890600	Enhancers	NHEK	skin
33	chr1:77890000-77890800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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