Variant report

Variant	rs9296105
Chromosome Location	chr6:33918063-33918064
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs59580109	1.00[AMR][1000 genomes]
rs9469639	1.00[AMR][1000 genomes]
rs9469651	0.93[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916210	chr6:33804111-34144062	Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
2	nsv462899	chr6:33880480-33944014	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv602841	chr6:33880480-33944014	Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers	Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33912600-33918800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr6:33914200-33918200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:33915400-33918400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr6:33917800-33919200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr6:33917800-33919600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:33917800-33919600	Enhancers	Fetal Intestine Small	intestine
7	chr6:33917800-33920000	Enhancers	Fetal Intestine Large	intestine
8	chr6:33918000-33918800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr6:33918000-33919000	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr6:33918000-33919200	Enhancers	Duodenum Mucosa	Duodenum
11	chr6:33918000-33919200	Enhancers	Rectal Mucosa Donor 29	rectum
12	chr6:33918000-33919400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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