Variant report

Variant	rs34994331
Chromosome Location	chr6:28047088-28047089
allele	-/AGAT
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Variant related genes	Relation type
ENSG00000198315	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000235109	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000219891	Chromatin interaction

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	nsv830619	chr6:27872302-28062544	Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
2	esv33436	chr6:28044346-28049043	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv823466	chr6:28046620-28048635	Weak transcription Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv823467	chr6:28046710-28048540	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	esv2621724	chr6:28047087-28047090	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
6	esv2105855	chr6:28047088-28047092	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28043200-28047800	Weak transcription	Spleen	Spleen
2	chr6:28045200-28047600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:28045600-28047800	Weak transcription	Right Atrium	heart
4	chr6:28045800-28047800	Weak transcription	Fetal Brain Male	brain
5	chr6:28046000-28047800	Weak transcription	Fetal Heart	heart
6	chr6:28046200-28047400	Enhancers	K562	blood
7	chr6:28046400-28047600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr6:28046600-28047400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr6:28046800-28047600	Enhancers	Primary B cells from peripheral blood	blood
10	chr6:28046800-28047600	Enhancers	Placenta	Placenta
11	chr6:28046800-28047800	Weak transcription	Left Ventricle	heart
12	chr6:28047000-28047200	Enhancers	Primary T helper cells PMA-I stimulated	--
13	chr6:28047000-28047200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr6:28047000-28047200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr6:28047000-28047600	Flanking Active TSS	GM12878-XiMat	blood
16	chr6:28047000-28047600	Enhancers	HepG2	liver
17	chr6:28047000-28047800	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr6:28047000-28047800	Weak transcription	Lung	lung
19	chr6:28047000-28048400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

Quick Search:

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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