Variant report

Variant	rs5752814
Chromosome Location	chr22:29230657-29230658
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr22:29227984..29230495-chr22:29230586..29232101,2	MCF-7	breast:
2	chr22:29167261..29170081-chr22:29228738..29231963,3	MCF-7	breast:
3	chr22:29221484..29225930-chr22:29227534..29231329,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000159873	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10427628	0.86[EUR][1000 genomes]
rs12170231	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5752808	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5752810	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5752811	0.93[AFR][1000 genomes]
rs5752815	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5762826	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5762829	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5762835	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5762838	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5762839	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5762848	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs5762852	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs5762855	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs5762858	0.83[EUR][1000 genomes]
rs5997409	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5997410	0.84[AMR][1000 genomes]
rs6005917	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9625591	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9625595	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9625600	0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1064079	chr22:29065528-29456059	Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	92 gene(s)	inside rSNPs	diseases
2	nsv834169	chr22:29095446-29303929	Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs5752814	XBP1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:29197200-29231600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr22:29198600-29231400	Weak transcription	HSMMtube	muscle
3	chr22:29198800-29230800	Weak transcription	NHEK	skin
4	chr22:29200600-29231400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr22:29214800-29242200	Weak transcription	Aorta	Aorta
6	chr22:29215600-29231600	Weak transcription	Right Ventricle	heart
7	chr22:29216000-29231600	Weak transcription	Placenta	Placenta
8	chr22:29216000-29232800	Weak transcription	Fetal Muscle Trunk	muscle
9	chr22:29216000-29233800	Weak transcription	Left Ventricle	heart
10	chr22:29216000-29238600	Weak transcription	Spleen	Spleen
11	chr22:29218200-29231800	Weak transcription	Gastric	stomach
12	chr22:29219400-29234800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr22:29219600-29231800	Weak transcription	Sigmoid Colon	Sigmoid Colon
14	chr22:29224000-29237400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr22:29225400-29242000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr22:29225800-29231600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr22:29225800-29231800	Weak transcription	HSMM	muscle
18	chr22:29225800-29233000	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr22:29226000-29231600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
20	chr22:29226000-29233000	Weak transcription	Dnd41	blood
21	chr22:29226000-29248800	Weak transcription	Primary T cells from cord blood	blood
22	chr22:29226200-29234600	Weak transcription	Brain Substantia Nigra	brain
23	chr22:29226200-29234800	Weak transcription	Duodenum Mucosa	Duodenum
24	chr22:29226200-29239600	Weak transcription	Rectal Mucosa Donor 29	rectum
25	chr22:29226200-29242800	Weak transcription	Stomach Smooth Muscle	stomach
26	chr22:29226400-29231600	Weak transcription	Pancreas	Pancrea
27	chr22:29226400-29231600	Weak transcription	Thymus	Thymus
28	chr22:29226600-29231800	Weak transcription	Fetal Intestine Large	intestine
29	chr22:29226600-29241800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr22:29226600-29242200	Weak transcription	Fetal Muscle Leg	muscle
31	chr22:29227800-29235000	Weak transcription	Liver	Liver
32	chr22:29228200-29231800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr22:29228200-29231800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr22:29228400-29231600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr22:29229400-29241800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr22:29230200-29231600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr22:29230400-29231600	Weak transcription	Lung	lung
38	chr22:29230400-29236800	Weak transcription	Fetal Stomach	stomach
39	chr22:29230600-29231600	Weak transcription	Fetal Intestine Small	intestine

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