Variant report

Variant	rs11911708
Chromosome Location	chr21:46123025-46123026
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs11908904	1.00[AFR][1000 genomes]
rs11910937	1.00[AFR][1000 genomes]
rs17213734	1.00[YRI][hapmap]
rs17286075	1.00[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
2	nsv913956	chr21:46096964-46279505	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
3	nsv1062245	chr21:46096964-46332587	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription 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	51 gene(s)	inside rSNPs	diseases
4	nsv544478	chr21:46096964-46332587	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Weak transcription Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46114400-46124400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr21:46118400-46123200	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr21:46118400-46123400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr21:46121400-46125200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr21:46121600-46123200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr21:46121600-46123800	Enhancers	H1 Cell Line	embryonic stem cell
7	chr21:46121800-46123200	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
8	chr21:46121800-46123600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr21:46121800-46124200	Enhancers	H9 Cell Line	embryonic stem cell
10	chr21:46121800-46124400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr21:46122200-46123200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr21:46122400-46123400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
13	chr21:46122800-46123200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr21:46122800-46123600	Flanking Bivalent TSS/Enh	HepG2	liver
15	chr21:46122800-46129400	Weak transcription	Right Atrium	heart
16	chr21:46123000-46124000	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
17	chr21:46123000-46124200	Enhancers	iPS DF 19.11 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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