Variant report

Variant	rs11816607
Chromosome Location	chr10:53017408-53017409
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs16913168	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16915917	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17173638	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7083539	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7083820	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7094420	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7097901	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7903693	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7903707	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7920480	0.96[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	nsv1036645	chr10:52804961-53159076	Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	22 gene(s)	inside rSNPs	diseases
2	nsv831874	chr10:53010357-53195508	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:53006800-53017600	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr10:53013000-53022800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr10:53015600-53019200	Weak transcription	Psoas Muscle	Psoas
4	chr10:53015600-53022600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr10:53016200-53021200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:53016600-53017600	Weak transcription	Rectal Smooth Muscle	rectum
7	chr10:53016600-53018000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr10:53017000-53017800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr10:53017000-53017800	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr10:53017000-53017800	Enhancers	NHLF	lung
11	chr10:53017000-53017800	Enhancers	Osteobl	bone
12	chr10:53017000-53018000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr10:53017000-53018000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
14	chr10:53017000-53018400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr10:53017000-53018400	Enhancers	Aorta	Aorta
16	chr10:53017000-53018400	Enhancers	NHDF-Ad	bronchial
17	chr10:53017000-53019000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr10:53017200-53017600	Enhancers	H1 Cell Line	embryonic stem cell
19	chr10:53017200-53017600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr10:53017200-53018000	Enhancers	HUES48 Cell Line	embryonic stem cell
21	chr10:53017200-53018200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr10:53017200-53018400	Enhancers	Fetal Muscle Leg	muscle
23	chr10:53017400-53017600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr10:53017400-53018000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr10:53017400-53018400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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