Variant report

Variant	rs141803986
Chromosome Location	chr8:68493026-68493027
allele	A/C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752263	chr8:68170946-68788493	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
2	nsv1024135	chr8:68235792-68629789	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv539642	chr8:68235792-68629789	Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv2752264	chr8:68244546-68647201	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
5	nsv1032986	chr8:68468044-68789883	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	nsv971662	chr8:68493011-68494892	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:68490600-68493400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr8:68491400-68493400	Enhancers	Primary T cells fromperipheralblood	blood
3	chr8:68491800-68493200	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr8:68491800-68493200	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr8:68492000-68493200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr8:68492000-68493200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr8:68492000-68493200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
8	chr8:68492200-68493200	Enhancers	Primary T cells from cord blood	blood
9	chr8:68492200-68493200	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr8:68492200-68493400	Enhancers	Primary T killer memory cells from peripheral blood	blood
11	chr8:68492400-68493200	Enhancers	GM12878-XiMat	blood
12	chr8:68492400-68493600	Enhancers	Dnd41	blood
13	chr8:68492600-68494400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr8:68492800-68493200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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