Variant report

Variant	rs1129771
Chromosome Location	chr7:26765596-26765597
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1024452	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1024453	0.91[CEU][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11971041	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11971098	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11972823	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11973332	1.00[CEU][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11976472	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11978456	1.00[CEU][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11979611	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11982489	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs213515	1.00[JPT][hapmap]
rs57579189	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57687803	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61609910	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6945204	0.87[EUR][1000 genomes]
rs6967749	1.00[CEU][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6970475	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs73683491	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73683496	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73683510	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs774265	1.00[JPT][hapmap]
rs7777645	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7780206	1.00[CEU][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7799519	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7809419	0.82[CEU][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.87[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	nsv1025538	chr7:26482342-27376045	Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
2	nsv538805	chr7:26482342-27376045	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS Genic enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	213 gene(s)	inside rSNPs	diseases
3	nsv1018125	chr7:26745074-26789814	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1129771	HOXA2	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:39 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:26731800-26779200	Weak transcription	Spleen	Spleen
2	chr7:26740400-26782400	Weak transcription	Fetal Intestine Small	intestine
3	chr7:26745000-26780800	Weak transcription	Aorta	Aorta
4	chr7:26746200-26780600	Weak transcription	Stomach Smooth Muscle	stomach
5	chr7:26746600-26777400	Weak transcription	Lung	lung
6	chr7:26749200-26779600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr7:26749600-26781000	Weak transcription	NHEK	skin
8	chr7:26750400-26812000	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:26753600-26782200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr7:26754200-26780600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr7:26754400-26782400	Weak transcription	Fetal Stomach	stomach
12	chr7:26754600-26780200	Weak transcription	NHLF	lung
13	chr7:26754800-26777000	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr7:26754800-26783200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr7:26755600-26782400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr7:26756200-26776800	Weak transcription	Dnd41	blood
17	chr7:26756600-26780600	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr7:26758400-26767200	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr7:26758400-26780800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:26758600-26767400	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr7:26759400-26775800	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr7:26761600-26766800	Strong transcription	Primary neutrophils fromperipheralblood	blood
23	chr7:26763000-26777600	Weak transcription	Fetal Lung	lung
24	chr7:26763000-26780600	Weak transcription	Primary T cells from cord blood	blood
25	chr7:26763200-26768400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr7:26763200-26769600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr7:26763200-26776600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:26763400-26768400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr7:26763600-26766400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr7:26763800-26776600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr7:26763800-26780600	Weak transcription	HMEC	breast
32	chr7:26764600-26766200	Strong transcription	Primary hematopoietic stem cells	blood
33	chr7:26764600-26767000	Strong transcription	Primary B cells from peripheral blood	blood
34	chr7:26764800-26766600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr7:26765000-26765800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr7:26765000-26766400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr7:26765000-26777000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr7:26765000-26778400	Weak transcription	Adipose Nuclei	Adipose
39	chr7:26765400-26767400	Strong transcription	Primary B cells from cord blood	blood

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