Variant report

Variant	rs58865277
Chromosome Location	chr1:59398116-59398117
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:59244053..59249750-chr1:59393075..59399809,12	K562	blood:
2	chr1:59246732..59251125-chr1:59394532..59399253,8	MCF-7	breast:
3	chr1:59244308..59248659-chr1:59395754..59399809,6	K562	blood:
4	chr1:59391994..59394040-chr1:59396746..59398985,2	MCF-7	breast:
5	chr1:59393493..59395224-chr1:59396747..59398606,2	MCF-7	breast:
6	chr1:59245645..59251479-chr1:59393366..59398471,10	MCF-7	breast:
7	chr1:59391656..59393565-chr1:59396729..59398732,3	K562	blood:

Variant related genes	Relation type
ENSG00000177606	Chromatin interaction
ENSG00000234807	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10158986	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10159430	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10889123	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11207340	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11207344	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11802596	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11803507	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13375549	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1886742	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs41287670	0.81[EUR][1000 genomes]
rs57136299	0.93[EUR][1000 genomes]
rs57438070	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58237960	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58289858	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60043252	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61414370	0.93[EUR][1000 genomes]
rs6667591	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6678724	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6693265	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72921508	0.93[EUR][1000 genomes]
rs72921540	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72921542	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72921578	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs744171	0.93[EUR][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	nsv1005354	chr1:59283572-59535812	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv829959	chr1:59340330-59503085	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv546316	chr1:59368947-59457815	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:59386600-59399800	Enhancers	Fetal Intestine Small	intestine
2	chr1:59388800-59398600	Weak transcription	Pancreas	Pancrea
3	chr1:59389000-59398800	Weak transcription	Right Atrium	heart
4	chr1:59389000-59407000	Weak transcription	Spleen	Spleen
5	chr1:59389200-59398600	Weak transcription	Psoas Muscle	Psoas
6	chr1:59389200-59401400	Weak transcription	Left Ventricle	heart
7	chr1:59390200-59399600	Enhancers	Placenta Amnion	Placenta Amnion
8	chr1:59391200-59399600	Enhancers	Fetal Intestine Large	intestine
9	chr1:59392000-59399600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr1:59392600-59398600	Weak transcription	Skeletal Muscle Male	skeletal muscle
11	chr1:59392600-59399400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr1:59393200-59398400	Weak transcription	Adipose Nuclei	Adipose
13	chr1:59393400-59398800	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr1:59393600-59398600	Weak transcription	Fetal Lung	lung
15	chr1:59393600-59400800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr1:59393600-59406800	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chr1:59393800-59398600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr1:59395400-59398400	Weak transcription	Rectal Smooth Muscle	rectum
19	chr1:59395400-59398600	Weak transcription	Gastric	stomach
20	chr1:59395400-59398800	Enhancers	NHEK	skin
21	chr1:59395600-59398800	Weak transcription	Colonic Mucosa	Colon
22	chr1:59395800-59398200	Enhancers	A549	lung
23	chr1:59395800-59398200	Weak transcription	HSMM	muscle
24	chr1:59395800-59400000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr1:59396000-59398200	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr1:59396000-59398400	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr1:59396000-59398400	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr1:59396000-59398400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
29	chr1:59396000-59398400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
30	chr1:59396000-59398600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr1:59396000-59398600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
32	chr1:59396000-59398600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
33	chr1:59396000-59398600	Weak transcription	Fetal Thymus	thymus
34	chr1:59396000-59400400	Enhancers	Hela-S3	cervix
35	chr1:59396200-59398200	Weak transcription	Duodenum Mucosa	Duodenum
36	chr1:59396200-59398400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr1:59396200-59398600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr1:59396400-59398400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
39	chr1:59396400-59398600	Weak transcription	Primary T cells from cord blood	blood
40	chr1:59396600-59398600	Weak transcription	Small Intestine	intestine
41	chr1:59396600-59399800	Enhancers	HMEC	breast
42	chr1:59397200-59398400	Enhancers	Monocytes-CD14+_RO01746	blood
43	chr1:59397200-59399000	Enhancers	Esophagus	oesophagus
44	chr1:59397200-59399400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr1:59397600-59398200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr1:59397600-59398800	Weak transcription	Stomach Mucosa	stomach
47	chr1:59397600-59399200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr1:59397600-59399400	Enhancers	Muscle Satellite Cultured Cells	--
49	chr1:59397600-59399400	Enhancers	NHDF-Ad	bronchial
50	chr1:59397600-59399600	Enhancers	Primary monocytes fromperipheralblood	blood

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