Variant report

No.	Distal block	Cell Line	Cell type
1	chr9:101121184..101122748-chr9:101132251..101134952,2	K562	blood:
2	chr9:101132158..101134151-chr9:101134451..101136659,2	MCF-7	breast:
3	chr9:101131416..101134090-chr9:101135125..101136966,2	MCF-7	breast:
4	chr9:101131978..101133928-chr9:101135656..101138427,3	K562	blood:
5	chr9:101130044..101133928-chr9:101135656..101137826,5	K562	blood:
6	chr9:101125471..101128354-chr9:101130836..101133824,3	MCF-7	breast:

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

rs_ID	r²[population]
rs10986071	0.82[JPT][hapmap]
rs10986073	0.85[JPT][hapmap]
rs16915442	0.85[JPT][hapmap]
rs2572364	0.82[CHB][hapmap]
rs3780428	0.80[CHB][hapmap]
rs3780429	0.80[CHB][hapmap]
rs3780430	0.80[CHB][hapmap]
rs473589	0.93[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs487910	0.95[CEU][hapmap];1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs531529	0.90[CHB][hapmap];0.81[ASN][1000 genomes]
rs552989	0.85[JPT][hapmap]
rs567931	1.00[CHB][hapmap];0.85[JPT][hapmap];0.81[ASN][1000 genomes]
rs585819	0.88[ASW][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.82[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs648085	1.00[CHB][hapmap];0.85[JPT][hapmap]
rs659768	0.80[CHB][hapmap]
rs660148	0.80[CHB][hapmap]
rs661105	0.85[JPT][hapmap]
rs661532	0.85[JPT][hapmap]
rs669095	0.82[CHB][hapmap]
rs670807	0.82[CHB][hapmap]
rs7047634	0.85[JPT][hapmap]

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	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831664	chr9:101024862-101205637	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101120600-101134400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr9:101126600-101142600	Weak transcription	Brain Angular Gyrus	brain
3	chr9:101127800-101134200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr9:101128200-101164200	Weak transcription	Brain Germinal Matrix	brain
5	chr9:101129000-101156000	Weak transcription	Fetal Brain Female	brain
6	chr9:101130400-101134800	Weak transcription	Brain Cingulate Gyrus	brain
7	chr9:101130800-101135600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr9:101131200-101135600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr9:101131400-101135200	Weak transcription	Osteobl	bone
10	chr9:101131400-101135400	Weak transcription	NH-A	brain
11	chr9:101132000-101134000	Weak transcription	K562	blood
12	chr9:101132600-101133000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:101132600-101133400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr9:101132600-101134600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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