Variant report

Variant	rs1886744
Chromosome Location	chr1:59396103-59396104
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:59244053..59249750-chr1:59393075..59399809,12	K562	blood:
2	chr1:59390738..59393434-chr1:59395453..59397807,2	MCF-7	breast:
3	chr1:59392641..59396388-chr1:59399124..59401431,3	K562	blood:
4	chr1:59246732..59251125-chr1:59394532..59399253,8	MCF-7	breast:
5	chr1:59244308..59248659-chr1:59395754..59399809,6	K562	blood:
6	chr1:59245645..59251479-chr1:59393366..59398471,10	MCF-7	breast:
7	chr1:59280123..59281954-chr1:59395680..59397207,2	MCF-7	breast:
8	chr1:59284595..59286940-chr1:59394772..59397437,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000177606	Chromatin interaction
ENSG00000234807	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11806596	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12071047	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12089816	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12093908	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17096897	1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs17118423	1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17118430	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17118441	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2477743	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2764909	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35393496	0.87[EUR][1000 genomes]
rs55675910	0.87[EUR][1000 genomes]
rs55834295	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55872264	0.87[EUR][1000 genomes]
rs56040345	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs56175432	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs56219110	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56251271	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56349902	0.87[EUR][1000 genomes]
rs58558886	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs66555203	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6681035	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72678885	0.87[EUR][1000 genomes]
rs72678896	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72678899	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72678900	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72678901	0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680106	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680107	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680109	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72680113	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72921571	0.88[EUR][1000 genomes];1.00[ASN][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:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:59385200-59397800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:59386600-59399800	Enhancers	Fetal Intestine Small	intestine
3	chr1:59388400-59397800	Weak transcription	NHLF	lung
4	chr1:59388600-59397800	Weak transcription	Lung	lung
5	chr1:59388800-59397800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr1:59388800-59398600	Weak transcription	Pancreas	Pancrea
7	chr1:59389000-59398800	Weak transcription	Right Atrium	heart
8	chr1:59389000-59407000	Weak transcription	Spleen	Spleen
9	chr1:59389200-59398600	Weak transcription	Psoas Muscle	Psoas
10	chr1:59389200-59401400	Weak transcription	Left Ventricle	heart
11	chr1:59390200-59399600	Enhancers	Placenta Amnion	Placenta Amnion
12	chr1:59391200-59399600	Enhancers	Fetal Intestine Large	intestine
13	chr1:59391600-59396200	Enhancers	Duodenum Mucosa	Duodenum
14	chr1:59391800-59396600	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr1:59392000-59397800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr1:59392000-59399600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr1:59392600-59396200	Enhancers	HMEC	breast
18	chr1:59392600-59398600	Weak transcription	Skeletal Muscle Male	skeletal muscle
19	chr1:59392600-59399400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:59393200-59398400	Weak transcription	Adipose Nuclei	Adipose
21	chr1:59393400-59397600	Weak transcription	Primary monocytes fromperipheralblood	blood
22	chr1:59393400-59398800	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr1:59393600-59397600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr1:59393600-59398600	Weak transcription	Fetal Lung	lung
25	chr1:59393600-59400800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr1:59393600-59406800	Weak transcription	Skeletal Muscle Female	skeletal muscle
27	chr1:59393800-59398600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr1:59394400-59396200	Bivalent Enhancer	HepG2	liver
29	chr1:59394400-59396600	Enhancers	Small Intestine	intestine
30	chr1:59394600-59396400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
31	chr1:59395000-59396200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr1:59395000-59396400	Enhancers	Primary T cells from cord blood	blood
33	chr1:59395000-59397600	Enhancers	Stomach Mucosa	stomach
34	chr1:59395200-59396200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
35	chr1:59395400-59398400	Weak transcription	Rectal Smooth Muscle	rectum
36	chr1:59395400-59398600	Weak transcription	Gastric	stomach
37	chr1:59395400-59398800	Enhancers	NHEK	skin
38	chr1:59395600-59397800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr1:59395600-59398800	Weak transcription	Colonic Mucosa	Colon
40	chr1:59395800-59397200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr1:59395800-59397200	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr1:59395800-59397600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr1:59395800-59397800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr1:59395800-59397800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:59395800-59397800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr1:59395800-59398000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
47	chr1:59395800-59398000	Weak transcription	Rectal Mucosa Donor 29	rectum
48	chr1:59395800-59398000	Weak transcription	NH-A	brain
49	chr1:59395800-59398200	Enhancers	A549	lung
50	chr1:59395800-59398200	Weak transcription	HSMM	muscle

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