Variant report

Variant	rs59301700
Chromosome Location	chr6:100791957-100791958
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:100777053..100778662-chr6:100790809..100792862,2	K562	blood:
2	chr6:100791372..100793069-chr6:100796170..100798348,2	K562	blood:

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs11962725	1.00[AMR][1000 genomes]
rs11964322	1.00[AMR][1000 genomes]
rs55692601	1.00[AMR][1000 genomes]
rs56176715	1.00[AMR][1000 genomes]
rs56876848	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57335321	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60973981	1.00[AMR][1000 genomes]
rs73760809	1.00[AMR][1000 genomes]
rs73760820	1.00[AMR][1000 genomes]
rs73760821	1.00[AMR][1000 genomes]
rs73760822	1.00[AMR][1000 genomes]
rs73760824	1.00[AMR][1000 genomes]
rs73760825	1.00[AMR][1000 genomes]
rs73760826	1.00[AMR][1000 genomes]
rs73760828	1.00[AMR][1000 genomes]
rs73760831	1.00[AMR][1000 genomes]
rs73760853	1.00[AMR][1000 genomes]
rs73760862	1.00[AMR][1000 genomes]
rs73760864	1.00[AMR][1000 genomes]
rs73760865	1.00[AMR][1000 genomes]
rs73760866	1.00[AMR][1000 genomes]
rs73760870	1.00[AFR][1000 genomes];1.00[AMR][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	nsv949535	chr6:100740293-101469052	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv1028122	chr6:100774245-100964347	Enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:100785600-100794000	Weak transcription	Psoas Muscle	Psoas
2	chr6:100787800-100794000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:100790000-100792200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr6:100790000-100792200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr6:100790000-100794600	Enhancers	HUVEC	blood vessel
6	chr6:100790600-100792000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr6:100790600-100793400	Enhancers	Dnd41	blood
8	chr6:100790600-100793400	Enhancers	HSMMtube	muscle
9	chr6:100790600-100794200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr6:100790600-100794400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr6:100790600-100794400	Enhancers	Osteobl	bone
12	chr6:100790600-100794600	Enhancers	NHDF-Ad	bronchial
13	chr6:100790800-100792000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:100790800-100792000	Enhancers	Skeletal Muscle Male	skeletal muscle
15	chr6:100790800-100793400	Enhancers	Fetal Heart	heart
16	chr6:100790800-100794200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr6:100790800-100794400	Enhancers	Skeletal Muscle Female	skeletal muscle
18	chr6:100790800-100794600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:100790800-100796800	Enhancers	HSMM	muscle
20	chr6:100790800-100796800	Enhancers	NH-A	brain
21	chr6:100791000-100792400	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr6:100791000-100792600	Weak transcription	Aorta	Aorta
23	chr6:100791200-100793000	Enhancers	Placenta Amnion	Placenta Amnion
24	chr6:100791200-100794000	Weak transcription	Hela-S3	cervix
25	chr6:100791400-100792200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr6:100791600-100792000	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chr6:100791800-100794800	Enhancers	NHLF	lung

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