Variant report

Variant	rs792453
Chromosome Location	chr10:22154208-22154209
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:22154173..22155847-chr10:22155964..22157700,2	K562	blood:

Extended variants
information (count: 72 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10508639	0.95[CEU][hapmap];1.00[CHB][hapmap];0.81[EUR][1000 genomes]
rs10740991	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs10764328	0.90[GIH][hapmap]
rs10764330	0.89[CEU][hapmap];0.95[MEX][hapmap];0.82[TSI][hapmap]
rs10828264	1.00[CHB][hapmap];0.85[GIH][hapmap]
rs10828266	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[MEX][hapmap]
rs10828283	0.81[EUR][1000 genomes]
rs1086896	0.87[EUR][1000 genomes]
rs1086899	0.80[CEU][hapmap];0.87[EUR][1000 genomes]
rs11012794	0.84[CEU][hapmap];1.00[CHB][hapmap];0.86[MEX][hapmap];0.87[ASN][1000 genomes]
rs1243179	0.87[ASN][1000 genomes]
rs1243194	1.00[CHB][hapmap];0.91[GIH][hapmap]
rs1243195	1.00[CHB][hapmap]
rs12571634	0.95[CEU][hapmap];0.80[TSI][hapmap];0.82[EUR][1000 genomes]
rs2026092	0.89[ASN][1000 genomes]
rs2066270	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.95[MEX][hapmap];0.92[TSI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2066271	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.95[MEX][hapmap];0.92[TSI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2252343	0.83[EUR][1000 genomes]
rs2457954	0.84[EUR][1000 genomes]
rs2487512	0.80[CEU][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap];0.88[EUR][1000 genomes]
rs2666750	0.80[CEU][hapmap];0.81[TSI][hapmap]
rs2666754	0.90[CEU][hapmap];0.91[GIH][hapmap];0.81[MEX][hapmap];0.81[AMR][1000 genomes]
rs2666756	0.81[CEU][hapmap]
rs2666757	0.94[CEU][hapmap];0.94[GIH][hapmap];0.81[MEX][hapmap];0.81[AMR][1000 genomes]
rs2666759	0.94[CEU][hapmap];0.82[EUR][1000 genomes]
rs2666768	0.95[CEU][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2666769	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.93[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2666771	0.95[CEU][hapmap];1.00[CHB][hapmap];0.95[MEX][hapmap];0.92[TSI][hapmap];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2666772	1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.81[MEX][hapmap];0.83[TSI][hapmap];0.84[EUR][1000 genomes]
rs2666775	0.95[CEU][hapmap];0.95[MEX][hapmap];0.87[TSI][hapmap];0.82[EUR][1000 genomes]
rs2666776	0.95[CEU][hapmap];0.94[GIH][hapmap];0.81[MEX][hapmap];0.81[AMR][1000 genomes]
rs2666779	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[GIH][hapmap];0.95[MEX][hapmap];0.92[TSI][hapmap];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2666782	0.95[CEU][hapmap];1.00[CHB][hapmap];0.85[EUR][1000 genomes]
rs2793341	0.82[EUR][1000 genomes]
rs2793351	0.82[EUR][1000 genomes]
rs2793352	0.82[EUR][1000 genomes]
rs2807968	0.89[CEU][hapmap];0.97[GIH][hapmap]
rs2807971	0.95[CEU][hapmap];1.00[CHB][hapmap];0.90[TSI][hapmap]
rs2807977	1.00[CHB][hapmap]
rs2807978	0.80[CEU][hapmap];0.80[EUR][1000 genomes]
rs2807979	0.95[CEU][hapmap];1.00[CHB][hapmap];0.81[TSI][hapmap];0.85[EUR][1000 genomes]
rs2807980	0.89[EUR][1000 genomes]
rs2807983	0.80[CEU][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs2807984	0.95[CEU][hapmap];1.00[CHB][hapmap];0.83[TSI][hapmap];0.85[EUR][1000 genomes]
rs2807985	1.00[CEU][hapmap];0.94[GIH][hapmap];0.85[TSI][hapmap];0.83[EUR][1000 genomes]
rs2807986	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs2807987	0.95[CEU][hapmap];0.81[MEX][hapmap];0.83[TSI][hapmap];0.84[EUR][1000 genomes]
rs2859622	0.85[CEU][hapmap]
rs2998360	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];0.81[MEX][hapmap];0.83[TSI][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs3951780	0.85[CEU][hapmap];1.00[CHB][hapmap]
rs4024198	0.95[CEU][hapmap];1.00[CHB][hapmap];0.85[MEX][hapmap];0.90[TSI][hapmap]
rs4146689	0.95[CEU][hapmap];1.00[CHB][hapmap];0.81[MEX][hapmap];0.80[TSI][hapmap];0.80[EUR][1000 genomes]
rs4364959	0.95[CEU][hapmap];0.91[GIH][hapmap];0.81[MEX][hapmap];0.82[TSI][hapmap]
rs4748775	0.94[CEU][hapmap]
rs4748776	0.95[CEU][hapmap];1.00[CHB][hapmap];0.91[GIH][hapmap];0.81[MEX][hapmap]
rs4748777	0.93[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes]
rs4748779	0.95[CEU][hapmap];0.81[MEX][hapmap];0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs7082663	0.89[CEU][hapmap];1.00[CHB][hapmap]
rs7089656	0.95[CEU][hapmap];1.00[CHB][hapmap];0.81[MEX][hapmap];0.83[TSI][hapmap];0.84[EUR][1000 genomes]
rs7904395	0.94[EUR][1000 genomes]
rs7910002	0.80[CEU][hapmap]
rs792454	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs792455	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs792456	0.89[CEU][hapmap];0.97[GIH][hapmap];0.86[MEX][hapmap];0.82[TSI][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs792457	0.88[EUR][1000 genomes]
rs792458	0.82[EUR][1000 genomes]
rs806772	0.84[EUR][1000 genomes]
rs806774	0.89[CEU][hapmap];1.00[CHB][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052464	chr10:21856531-22220087	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
2	esv1802317	chr10:21866085-22288132	Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	esv1793816	chr10:22088054-22285371	Strong transcription Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv3693050	chr10:22154208-22160986	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active 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
rs792453	MLLT10	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22124200-22169800	Weak transcription	Right Ventricle	heart
2	chr10:22124400-22163000	Weak transcription	Ovary	ovary
3	chr10:22126200-22161800	Weak transcription	Left Ventricle	heart
4	chr10:22126600-22161800	Weak transcription	Pancreas	Pancrea
5	chr10:22133000-22157800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr10:22133400-22161000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr10:22137600-22159400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr10:22138000-22161400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr10:22139000-22161200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr10:22139200-22161200	Weak transcription	Fetal Lung	lung
11	chr10:22140000-22159800	Weak transcription	Stomach Smooth Muscle	stomach
12	chr10:22140600-22159400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr10:22140600-22159600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr10:22140800-22156400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr10:22140800-22169800	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr10:22140800-22174800	Weak transcription	HSMM	muscle
17	chr10:22141600-22157400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr10:22142200-22161200	Weak transcription	Primary T helper cells fromperipheralblood	blood
19	chr10:22148600-22161600	Weak transcription	K562	blood
20	chr10:22149600-22180200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr10:22150200-22155600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr10:22150600-22155400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr10:22150600-22160000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr10:22151800-22156200	Weak transcription	Fetal Brain Male	brain
25	chr10:22152200-22161000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr10:22152600-22156400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr10:22153000-22169800	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr10:22153000-22200600	Weak transcription	Osteobl	bone
29	chr10:22153200-22161000	Weak transcription	Fetal Stomach	stomach
30	chr10:22154000-22158800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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