EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS082-14600 
Organism
Homo sapiens 
Tissue/cell
HCASMC 
Coordinate
chr17:29891380-29892280 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs62063930chr1729891429hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CDX2MA0465.1chr17:29891789-29891800TTTTATGGCTC-6.14
SP2MA0516.2chr17:29891896-29891913CAGGGGGCAGGGCTTAC-6.08
SREBF2MA0596.1chr17:29891993-29892003ATCACCCCAT-6.02
ZNF263MA0528.1chr17:29892229-29892250GGAGGATGGGAGGGCTGGGGG+6.11
Number of super-enhancer constituents: 11             
IDCoordinateTissue/cell
SE_00097chr17:29884943-29903384Adipose_Nuclei
SE_27382chr17:29891001-29891598Esophagus
SE_27382chr17:29891625-29893307Esophagus
SE_33988chr17:29890922-29894815HCC1954
SE_37031chr17:29890703-29893725HSMMtube
SE_44284chr17:29890720-29893125NHDF-Ad
SE_45081chr17:29892146-29893094NHLF
SE_45954chr17:29890579-29902407Osteoblasts
SE_47701chr17:29891335-29892414Pancreas
SE_55681chr17:29890501-29900599u87
SE_65467chr17:29890939-29893536Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr172989213429892258
Number: 1             
IDChromosomeStartEnd
GH17I031563chr172989092229896350
Enhancer Sequence
GCAGCCTCCC AGGTCGGAAG CCAGCAAGCT GGGGCTGTAG AACAGGAGGT GGCTGGGCCT 60
GGATTCGCTG GCACTGAGTC CTTAAAGGAA CCCTGGGTAG CAGATGTGGC CGCCTTGTAC 120
ATCTGCTCAG CAGTGCATCA CTCCTAAAGG CCCAAAGACT CGTCCGGTCC TGACACTGAG 180
CACGTTTCAG AAAAGGTCCC AGGAAAGACA TTTGAATTGC CACAGCTGCT CAAGGCTTGC 240
TCCCTCACTC ATGCTGTGGG CAAACTAAAC ATCCTCTAGT GGGACCAGGC AAGCAGGGGA 300
CAAAATGGAA TGGGGGTGCG GGGGAGGAGA AAATAATTTG ATATTCCAAA AAATGCTGCA 360
GAGTAATCAT TTTGGGGGTG AAAATCAGAA TTTCTTGGGA CTTAGACTTT TTTATGGCTC 420
AGTGGTGTTT TTCTTTAGAA TTTTGGACTG GAGGTAGGGA TAGACCATAA TCTTTTCAGC 480
ACCCAAGAGC CTTCAGCAGG CCTCACTGGC TCTGGGCAGG GGGCAGGGCT TACAGGACCC 540
AGAGCAGGTG ACATCTTACC CACTGTGGAT ACTTCCTCCC TCCTCCCTTT GGCACGGTCT 600
GAGGAATTTT GAAATCACCC CATAGCCAGA CCCCTTGCAT TTGCTGCCCA GGAGAACCGG 660
GCAGGGAGGT GCCATGCGGA AAGTCCCGCT GCCTGATTTT CCTCTGAGCT CATCACTGCA 720
GCCTGAGAGC CCCCTTCTCT GTCAAGTGGG TGACTGAACT GAATACACCA GACCCCCCTT 780
GGCATTCTTC TAAGATCCTA AGGAGGAGGA GCTGAGGAAG GCACGGGGTG GAGCCTGGGG 840
CTGTGGTTTG GAGGATGGGA GGGCTGGGGG AGGGATTCAG AGATTGCAGC TGGGAAATTT 900