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

TagContent
EnhancerAtlas ID
HS138-00178 
Organism
Homo sapiens 
Tissue/cell
MSC_BM 
Coordinate
chr1:12045590-12046640 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs2336384chr112046063hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr1:12045743-12045758TGAACTCCTGACCTC-6.22
Number of super-enhancer constituents: 5             
IDCoordinateTissue/cell
SE_28500chr1:12037809-12046747Fetal_Intestine
SE_29466chr1:12037756-12047000Fetal_Intestine_Large
SE_40992chr1:12038203-12047280Left_Ventricle
SE_42819chr1:12045532-12046902Lung
SE_49145chr1:12045709-12046770Right_Atrium
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr11204595912046248
chr11204629912046451
chr11204602312046196
Enhancer Sequence
TTGGCTCACT GCAAATTCTA CCTCCCAGGT TCAAGTGATT CTCCTGCCTT GGCCTCTGGA 60
GTAGCTGGGA CTACAGGCAT GCGCCACCAC ACCCAGCTAA TTTTTTGTAT TTTTCATAGA 120
GACGGGGTTT CACCATGTTG GCTAGACTGG TCTTGAACTC CTGACCTCAG GTGAGCTGCC 180
TGCCTCGGCC TCCCAAAGTG CTGGGATTAC AGGCATGAGC CACCGTGCCT GACCCCTGAT 240
CCCTTTTCTA TTCCTTTTGG ATGGCTTTCC TCTTGTGCCT GCCACATCCC CTCTTTCTCG 300
AACAGTCTGA TCTGCCAGGC CATGGCAAGC CTCATTTCAG CGCACTCTCC TTTGCTGCTT 360
TGGAAGAGTG AGAGTAGCAT TTTCTTTGCA GTTTCCTTTC TCAGAGCTGT ACTGTCTTTA 420
AGCCCTGGAC ATATGGCTTC CATGCTGAGA AAACATCTCT CATAGCTGTG GCGTCATGCT 480
GAGGAGGAAT GTAGAAACGG AAGTGGGGTC ACTTCCTTCC CTTGTCTCCA GAGGAATCAT 540
TAACATTGCA CAAGAACTTG TTGGTTTGGG CACACATGTG GGTCCCTATC CCGCTTTGGG 600
TCGGTCTGTC TTCTGCCCAC TCTTTGGGAT GGTTAGTTAC TAAAAGTCCG TTTTGGCATT 660
TGGTCTTCAT GTACCTCTTC CGGGTGTTCT TTCTGCTTTT CAGGACCTTG TGCAACATAC 720
TTTGGCCCCA TTTGGAAGTT TTTCACGTGT GCTTGCTGGG GAGCAACACC TCATTTCCAA 780
TCTAGAGAGA GTGAGCTTAC TGCTGGGTGG AGAACTGAGC AGTAAGATTA GGGTGGCTGG 840
GGAGGCAGTG ACAGACCCAG GCACAGTCAG CTGTGCACAC ACCCCCTCAT CCAGGAGGGC 900
CTTTGCCCTT TGACTTCCTG GGATTGGTGG GCTCTGCTCA AGAAGTAGCT TTCGCCGTGG 960
TGGGAACTCT GAGGGACCTG GCAGGGGTCC ACTTTTGGGG TCGGAATTCC CAGTCTTACC 1020
CTGGGCACTC CTTCTGGTGT GTACGCCTCT 1050