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

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EnhancerAtlas ID
HS073-00255 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr1:25466180-25467330 
Target genes
Number: 9             
NameEnsembl ID
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs9803723chr125466629hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:25467070-25467088GGAAGGAAGCCCGGCAGG+6.35
Foxd3MA0041.1chr1:25466199-25466211GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr1:25466203-25466215GTTTGTTTGTTT+6.32
Foxd3MA0041.1chr1:25466207-25466219GTTTGTTTGTTT+6.32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12546672525467101
Number: 1             
IDChromosomeStartEnd
GH01I025140chr12546672525467101
Enhancer Sequence
TGTTTTTTTT GTTTTTTTTG TTTGTTTGTT TGTTTGTTTT GAGACAGGAT CTAGCTCCAT 60
TACCCAGCCC AGATCTAGCT CTGTCCGCCG AATGGTGTGA TCACAGCTCA CTGCAGCCTC 120
AGCTTCAACT GCCTGGACTT AAGCGATCCT CCCACCTCAG CCTCCTGAGA AGCTAGGACC 180
AGAGCCATCC ACCCATGCCA AGCTAATTTT TAAATTTTTT TGCAGAAACG AGGTCTCACT 240
ATGTTGCCCA GGCTAGTCTT GAACTCCTGG GCTCAAGCGA TCGTCCCACC TCAGCCTCCC 300
AGAGTGTTGG GATTACAGGC ATGAGCCACC GTGCCTGACC AAGATCTTTA AATAGTAATA 360
AAACAGACAT TTATTAAGTG CATCTCATGT GCTGTGCGCT GTTCCAAGTG CCTACACTCC 420
CCATCTCAGT TAAGCACACA CCACCCCACG GGCAGGCAGC TGCTATCATT ATCCCTTTCT 480
CATGGTGGGG AAGTGAAGAT CAGAAAGGCT GAATAACTTG CTCAAGATCA CAAGTCTGGA 540
CTTGACTGCA GGCCTGGCTG ATCCCAGAGC CCAGATCAAG AGTCTCCCCT GGTGCCTCTC 600
CCCTAAAACC ACCTCAGAAA CCCCCTGGTG TGTAACTCTA AACCATGCCT GCGGCAAACT 660
CAGCCCATTT CCTCTTCTCG CATCTTAAGC CCAGATGGGG TCTGAGTGAC ACTTATCTCA 720
TACCCTGTCA TAGAGCTGGA GCCCCACAGG AATGTGGAAC TCCCCATGGA CAGAGGGCAG 780
GAGGAAGTGA CCGCCGGCCC GAAGGGGGCT TGGTCCACTG GGTCCAAAGG TGCCGTCTGG 840
CCCTGGCTGC CACATGCCTC GTGTCCACAA AGCAGAAGTC ACAGGGACAG GGAAGGAAGC 900
CCGGCAGGCA GACTGTCATC ACAGGTGGTG TGTCCTCCTA TCCAGGGACA AGCAGAACTA 960
GCCAAGATTG CCTTCTCCAC GCAGCCTCTC CTGATTCCAC ACTTGTGACT TCATGTTCCC 1020
AGAGCGCTGT GCTGGCACGT GTGCTATGAT CTTGACTCTG TATGCACCCC GACGCCCAGC 1080
TACAAGCAGC TCTACCCTTA CCTAACCTTT AAATTGCTCG ATTGCCTCAT CTGTAAAAAC 1140
AGGGATGTTA 1150