Variant report

Variant	rs540664374
Chromosome Location	chr6:11689148-11689149
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

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	esv2758036	chr6:11679753-11822351	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	esv2759407	chr6:11679753-11822351	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv428470	chr6:11686198-11747850	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv981310	chr6:11689104-11694850	Weak transcription Strong transcription ZNF genes & repeats Enhancers Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:11685000-11689400	Enhancers	Fetal Intestine Large	intestine
2	chr6:11685200-11693000	Weak transcription	Spleen	Spleen
3	chr6:11686600-11701400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:11686600-11702400	Weak transcription	HSMMtube	muscle
5	chr6:11687200-11689200	Enhancers	Fetal Heart	heart
6	chr6:11687200-11689200	Enhancers	Fetal Stomach	stomach
7	chr6:11687200-11689400	Enhancers	Brain Germinal Matrix	brain
8	chr6:11688600-11689200	Enhancers	Fetal Kidney	kidney
9	chr6:11688600-11689200	Enhancers	Fetal Lung	lung
10	chr6:11688600-11689400	Enhancers	Fetal Intestine Small	intestine
11	chr6:11688600-11689400	Enhancers	Ovary	ovary
12	chr6:11688800-11692600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:11688800-11711000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr6:11689000-11689800	Strong transcription	HSMM	muscle

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Input of quick search could be:

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

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