EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS105-29388 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr16:1296920-1297800 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4984778chr161297516hg19
TF binding sites/motifs
Number: 38             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr16:1296979-1296997GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr16:1296983-1297001GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr16:1296987-1297005GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr16:1296991-1297009GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr16:1296995-1297013GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr16:1296999-1297017GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr16:1297003-1297021GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr16:1297007-1297025GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr16:1297011-1297029GGAAGGAAGGAAGGAAGG+10.83
EWSR1-FLI1MA0149.1chr16:1296932-1296950GGAGGGAGGGAAAGAAAG+6.31
EWSR1-FLI1MA0149.1chr16:1296936-1296954GGAGGGAAAGAAAGAAGG+6.56
EWSR1-FLI1MA0149.1chr16:1296924-1296942AGAAGGAAGGAGGGAGGG+6.62
EWSR1-FLI1MA0149.1chr16:1296956-1296974GGAAGGAAGGAGAGAAAG+6.94
EWSR1-FLI1MA0149.1chr16:1296928-1296946GGAAGGAGGGAGGGAAAG+7.5
EWSR1-FLI1MA0149.1chr16:1296944-1296962AGAAAGAAGGAAGGAAGG+7.85
EWSR1-FLI1MA0149.1chr16:1296940-1296958GGAAAGAAAGAAGGAAGG+7.87
EWSR1-FLI1MA0149.1chr16:1297015-1297033GGAAGGAAGGAAGGGAGA+8.31
EWSR1-FLI1MA0149.1chr16:1296920-1296938GGAAAGAAGGAAGGAGGG+8.34
EWSR1-FLI1MA0149.1chr16:1296952-1296970GGAAGGAAGGAAGGAGAG+8.99
EWSR1-FLI1MA0149.1chr16:1296948-1296966AGAAGGAAGGAAGGAAGG+9.09
EWSR1-FLI1MA0149.1chr16:1296975-1296993GAAAGGAAGGAAGGAAGG+9.6
IRF1MA0050.2chr16:1296964-1296985GGAGAGAAAGAGAAAGGAAGG-6.1
ZNF263MA0528.1chr16:1296976-1296997AAAGGAAGGAAGGAAGGAAGG+6.16
ZNF263MA0528.1chr16:1296933-1296954GAGGGAGGGAAAGAAAGAAGG+6.75
ZNF263MA0528.1chr16:1296949-1296970GAAGGAAGGAAGGAAGGAGAG+6.76
ZNF263MA0528.1chr16:1297016-1297037GAAGGAAGGAAGGGAGAGGGG+6.78
ZNF263MA0528.1chr16:1296925-1296946GAAGGAAGGAGGGAGGGAAAG+6.79
ZNF263MA0528.1chr16:1297012-1297033GAAGGAAGGAAGGAAGGGAGA+6.85
ZNF263MA0528.1chr16:1296957-1296978GAAGGAAGGAGAGAAAGAGAA+6.93
ZNF263MA0528.1chr16:1296980-1297001GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr16:1296984-1297005GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr16:1296988-1297009GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr16:1296992-1297013GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr16:1296996-1297017GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr16:1297000-1297021GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr16:1297004-1297025GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr16:1297008-1297029GAAGGAAGGAAGGAAGGAAGG+6.94
ZNF263MA0528.1chr16:1296929-1296950GAAGGAGGGAGGGAAAGAAAG+7.68
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1612970361297134
Enhancer Sequence
GGAAAGAAGG AAGGAGGGAG GGAAAGAAAG AAGGAAGGAA GGAAGGAGAG AAAGAGAAAG 60
GAAGGAAGGA AGGAAGGAAG GAAGGAAGGA AGGAAGGAAG GAAGGAAGGG AGAGGGGGTT 120
ATCCCGTAGC TCTGCCGTAT AGCCAGTCAG CCCTGAAGTA GCTGTGGGCA TCCTACTGAC 180
ATGTAATTCT CAATCGCCAA ATCCAAGTCC ATCAGCTCTC CCAAAAATGT CCTTGGATGG 240
AAAATGTCCT GCCTAGGATC AGGAGGCACG CTGGGCTCTG GAACGGGTCC TCGGTCTTTC 300
CTCAGCTCCT CTGACCCTGA GACCCTTGAA GATTTCGGGC CATCGTTTTG TGGAGCGCTC 360
CTCAAGCCGG GCTGATATTT TTTCACGATT AGATTGAGGG GATACCCGTT TGGCAGGAGC 420
ATCACAGGCC CGGCTCTGAG GTCCGCCTCC TGTCAAGGGC GTGCACGACC GACTTCTCCA 480
GTTGCTGGGA CATCCACTCT CATCTCTTGA GCAAGGGGCA TCTGCCCGGC TTCTCCCCGG 540
GAAGCCACTC CTTCCCCTTA GTGATGACTG CGTGTTTTGT GGGGAGATTC CTTGACACCC 600
TGTAACTAGC CAAGTTCTCA TCAGACTATG TATTCATTTG CTTATTTATA ACTGTATAGA 660
CTCATGGTCC CCTGTTTTAT TCAGTTATTT TAATTTCTTT CTTTTTCCCA ATCATTTTAT 720
AATGTGCAAA CTCGCTCTGA TGCGGACACT GGGAGCTCCT GCGAGCTGGC TTCTGTGTCA 780
TCTGACATGT CTCCGTCTCT GAACTTTTCC TCCTACAAGA TTCTTCTGGG CTCCTCTCAT 840
ATCCGCCTCT GCGCCAGGCA GTCCTCCAGG AGGCCCAGCT 880