Variant report

Variant	rs7091558
Chromosome Location	chr10:91093145-91093146
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:91086403..91089519-chr10:91091273..91094339,4	K562	blood:

Variant related genes	Relation type
ENSG00000119917	Chromatin interaction

Extended variants
information (count: 83 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10159512	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10159516	0.85[AMR][1000 genomes]
rs10159652	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10159694	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10159869	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10159879	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1041540	1.00[ASN][1000 genomes]
rs11203074	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11203075	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11203076	0.85[AMR][1000 genomes]
rs11203077	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11203081	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11203084	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11203085	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11203087	0.85[AMR][1000 genomes]
rs11203088	1.00[ASN][1000 genomes]
rs11203097	1.00[ASN][1000 genomes]
rs12241343	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12242568	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12244506	0.85[AMR][1000 genomes]
rs12244571	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12245627	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12249661	1.00[ASN][1000 genomes]
rs12249707	1.00[ASN][1000 genomes]
rs12250753	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12250860	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12251895	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12259713	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12259768	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12261273	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12263989	1.00[ASN][1000 genomes]
rs12264051	1.00[ASN][1000 genomes]
rs12266581	1.00[CEU][hapmap];1.00[AMR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12267943	1.00[ASN][1000 genomes]
rs1332332	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1332333	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1332334	0.85[AMR][1000 genomes]
rs1332336	0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1332337	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17119593	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17119665	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17119672	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17119790	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17119791	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2151008	1.00[ASN][1000 genomes]
rs41284140	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41284142	1.00[ASN][1000 genomes]
rs4378299	1.00[ASN][1000 genomes]
rs6586185	0.85[AMR][1000 genomes]
rs6586186	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6586187	0.85[AMR][1000 genomes]
rs6586189	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6586190	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6586191	1.00[ASN][1000 genomes]
rs7081163	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7088379	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7099668	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7099681	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7100115	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73367441	0.85[AMR][1000 genomes]
rs73367444	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73367447	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73367460	0.85[AMR][1000 genomes]
rs73368528	0.85[AMR][1000 genomes]
rs7898580	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7901862	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7902096	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7902109	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7902380	0.85[AMR][1000 genomes]
rs7904924	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7906827	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7907341	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7911396	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7916398	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7917725	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9663337	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9663529	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9663533	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv1041964	chr10:90861380-91378356	Flanking Active TSS Enhancers Weak transcription Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
4	nsv1040375	chr10:91022218-91153074	Enhancers Active TSS Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	esv34085	chr10:91065949-91174175	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 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	chr10:91087200-91093600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr10:91088000-91099800	Weak transcription	Gastric	stomach
3	chr10:91088200-91093200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr10:91088200-91093400	Weak transcription	Esophagus	oesophagus
5	chr10:91090200-91107600	Weak transcription	Pancreas	Pancrea
6	chr10:91091200-91094000	Enhancers	Fetal Brain Male	brain
7	chr10:91091600-91093400	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
8	chr10:91091600-91094200	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr10:91091800-91093200	Flanking Active TSS	Primary hematopoietic stem cells	blood
10	chr10:91091800-91093200	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
11	chr10:91091800-91093200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr10:91091800-91093200	Flanking Active TSS	Brain Hippocampus Middle	brain
13	chr10:91091800-91093200	Active TSS	Ovary	ovary
14	chr10:91091800-91093200	Flanking Active TSS	HepG2	liver
15	chr10:91091800-91093400	Flanking Active TSS	Brain Substantia Nigra	brain
16	chr10:91091800-91093400	Flanking Active TSS	Osteobl	bone
17	chr10:91091800-91093600	Flanking Active TSS	Primary T cells from cord blood	blood
18	chr10:91091800-91093600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
19	chr10:91091800-91093600	Flanking Active TSS	NHEK	skin
20	chr10:91091800-91093800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
21	chr10:91091800-91093800	Flanking Active TSS	Primary B cells from cord blood	blood
22	chr10:91091800-91094000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr10:91091800-91094000	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr10:91091800-91094000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr10:91091800-91094000	Flanking Active TSS	Brain Anterior Caudate	brain
26	chr10:91091800-91094200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr10:91091800-91094200	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
28	chr10:91091800-91094200	Flanking Active TSS	Adipose Nuclei	Adipose
29	chr10:91091800-91094200	Flanking Active TSS	Liver	Liver
30	chr10:91091800-91094200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr10:91092000-91093200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr10:91092000-91093200	Active TSS	Right Ventricle	heart
33	chr10:91092000-91093200	Flanking Active TSS	A549	lung
34	chr10:91092000-91093400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr10:91092000-91094000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr10:91092000-91094000	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr10:91092000-91094000	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
38	chr10:91092000-91094200	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr10:91092000-91094200	Enhancers	HUES48 Cell Line	embryonic stem cell
40	chr10:91092000-91094200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
41	chr10:91092000-91094200	Flanking Active TSS	Fetal Thymus	thymus
42	chr10:91092200-91093200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
43	chr10:91092200-91093200	Active TSS	Lung	lung
44	chr10:91092200-91093200	Flanking Active TSS	HSMMtube	muscle
45	chr10:91092200-91093400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
46	chr10:91092200-91093400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr10:91092200-91093400	Flanking Active TSS	Brain Cingulate Gyrus	brain
48	chr10:91092200-91093600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr10:91092200-91094000	Enhancers	Fetal Heart	heart
50	chr10:91092200-91094200	Enhancers	H9 Cell Line	embryonic stem cell

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