Variant report

Variant	rs7100644
Chromosome Location	chr10:97628438-97628439
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs10509697	1.00[CHB][hapmap]
rs11188419	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11188423	0.88[JPT][hapmap]
rs11188424	0.83[EUR][1000 genomes]
rs11188431	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11188433	0.88[JPT][hapmap]
rs11188448	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11188450	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11188451	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11188461	0.82[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs11188466	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11188467	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11188469	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11188475	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11188479	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11188481	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11188491	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11188502	1.00[CEU][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11188508	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11553577	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes]
rs11819621	1.00[CHB][hapmap]
rs11819652	1.00[CHB][hapmap]
rs12355114	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12357211	0.80[EUR][1000 genomes]
rs12358517	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12784530	0.88[JPT][hapmap]
rs1414914	1.00[CHB][hapmap]
rs2275760	1.00[CEU][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2901895	1.00[CHB][hapmap]
rs3176882	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3181121	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3818833	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs41291576	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4420188	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4512762	0.87[ASN][1000 genomes]
rs56747025	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs57456033	0.90[AMR][1000 genomes]
rs58169787	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59502315	0.93[ASN][1000 genomes]
rs60144080	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs61503377	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs61731067	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7070507	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7073937	1.00[JPT][hapmap]
rs7090630	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7093453	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73315224	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73315254	0.93[ASN][1000 genomes]
rs73315260	0.97[ASN][1000 genomes]
rs73315285	0.87[ASN][1000 genomes]
rs73317145	0.87[ASN][1000 genomes]
rs73329287	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs73331134	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73333021	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7898422	0.97[ASN][1000 genomes]
rs7907476	1.00[CHB][hapmap]
rs7909124	1.00[CHB][hapmap]
rs7912552	1.00[CHB][hapmap]
rs7913155	0.97[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	nsv531923	chr10:97366055-97725757	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv895905	chr10:97513362-97686064	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv895906	chr10:97513362-97703650	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv895907	chr10:97529318-97686064	Weak transcription Enhancers Strong transcription Active TSS 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	10 gene(s)	inside rSNPs	diseases
5	nsv895908	chr10:97544513-97724247	Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:97592600-97632800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr10:97600600-97628600	Weak transcription	Colonic Mucosa	Colon
3	chr10:97601600-97635600	Weak transcription	Fetal Brain Male	brain
4	chr10:97601800-97635400	Weak transcription	Brain Substantia Nigra	brain
5	chr10:97601800-97647800	Weak transcription	Brain Cingulate Gyrus	brain
6	chr10:97602400-97655400	Weak transcription	Skeletal Muscle Male	skeletal muscle
7	chr10:97615400-97634400	Strong transcription	Primary monocytes fromperipheralblood	blood
8	chr10:97615800-97633800	Strong transcription	Primary neutrophils fromperipheralblood	blood
9	chr10:97615800-97634400	Strong transcription	Monocytes-CD14+_RO01746	blood
10	chr10:97618000-97631200	Weak transcription	Psoas Muscle	Psoas
11	chr10:97619000-97631000	Weak transcription	Adipose Nuclei	Adipose
12	chr10:97619400-97633000	Weak transcription	Fetal Brain Female	brain
13	chr10:97619600-97655000	Weak transcription	HUVEC	blood vessel
14	chr10:97619800-97633400	Weak transcription	A549	lung
15	chr10:97620800-97633000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr10:97621000-97628600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr10:97621000-97640600	Weak transcription	Rectal Smooth Muscle	rectum
18	chr10:97621000-97666800	Weak transcription	Gastric	stomach
19	chr10:97622200-97631800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
20	chr10:97622400-97632000	Weak transcription	Lung	lung
21	chr10:97622800-97631600	Weak transcription	Primary hematopoietic stem cells	blood
22	chr10:97622800-97666600	Weak transcription	Thymus	Thymus
23	chr10:97623800-97666600	Weak transcription	Right Ventricle	heart
24	chr10:97624200-97631800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr10:97624600-97632000	Weak transcription	Spleen	Spleen
26	chr10:97624800-97635000	Weak transcription	Small Intestine	intestine
27	chr10:97625000-97630000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr10:97625000-97631600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr10:97625000-97631600	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr10:97625000-97632200	Weak transcription	Fetal Lung	lung
31	chr10:97625000-97632800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr10:97625000-97633000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr10:97625000-97633200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr10:97625000-97634200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr10:97625200-97630000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr10:97625200-97630000	Weak transcription	Fetal Stomach	stomach
37	chr10:97625200-97631200	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr10:97625200-97632000	Strong transcription	GM12878-XiMat	blood
39	chr10:97625200-97634200	Weak transcription	H9 Cell Line	embryonic stem cell
40	chr10:97625200-97635800	Weak transcription	Primary T helper cells PMA-I stimulated	--
41	chr10:97625200-97636800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr10:97625200-97655200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr10:97625400-97630200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr10:97625400-97648600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
45	chr10:97625400-97649200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr10:97625400-97666400	Weak transcription	Osteobl	bone
47	chr10:97625600-97631400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr10:97625600-97633400	Strong transcription	Primary B cells from peripheral blood	blood
49	chr10:97625800-97628800	Strong transcription	Aorta	Aorta
50	chr10:97625800-97628800	Strong transcription	Left Ventricle	heart

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