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

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EnhancerAtlas ID
HS176-31941 
Organism
Homo sapiens 
Tissue/cell
SK-N-SH 
Coordinate
chr5:79405140-79406320 
Target genes
Number: 1             
NameEnsembl ID
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr5:79405975-79405996CCTCCTCCTCCCTGCTCCCCC-6.65
ZNF263MA0528.1chr5:79405972-79405993TCTCCTCCTCCTCCCTGCTCC-7.16
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr57940545979406276
Number: 1             
IDChromosomeStartEnd
GH05I080109chr57940551779407982
Enhancer Sequence
TGCACCACCA GGCCCGGCTA ATTTATATAT ATATATATAT TTTTAGCAGA GACAGGTTTT 60
TACCATGTTG GCCAGGCTGG TCTTGAACTC CTGCCCTCAA GTGATCCACC TGCCTTGGCC 120
TCCCAAAGTA CTGGGATTAC AGGCATGAGC CACTGGGCCT GGCTGGCATT TCTGCATTTT 180
TAATACCTTG GGAACAACCA CCACCCCTCA AAATGACAGT GGCTCATCTT TGTCAATTAT 240
ACCTTAATAA AGCTGGAGGA AAATTAATAA AATGGACTAC AAAAGAAGAA GAAGAAGAAG 300
AAGAAGAAAA GAAAAGAAAG TAGCCCAAGT TCTCTGTACC TCCCAGATGC CCCAGTGAAG 360
GGCCTCAGCT GTGATGAGAA AACCCAGCAG CCCAATTCCT GGCAACTCTC CTGGGATCTG 420
GAATGATGGT GTGCCTGGGC ACAGCCTTCC TATCTGGCCC GAGAGCCAGC TGGCACCATT 480
GGAGTGAGGA GAGGGCTCTG AGCTTTCCCA GTAGGCTGGC AACCTCCCAG GCTCCCTCCC 540
CCAGCCCCTA TAAAACCATC TGGAAAATGA AAATAATACC TTCTGCTTCC TACCAAGCTC 600
CAGGGACCCT GTGAGGAACA GGGAGATACT ATCCCCATAC CCCACACATT CCTGGAGGAG 660
GTTGCCCTGG AATAAGCTAT TGCCCCGCCT CTTTCACCCC AAGTGGCAGA AACGAGGGCC 720
ACTCAGTGCT CTGTCCAGCT GCTCTTGCTT CCCCTCAGGA GCCACTTCTG CTTCCATCCC 780
ACCTGATTGG AGTGGGCTTC CCACAGGCCC CCGCTCCGCA GCTCCTCAGT GCTCTCCTCC 840
TCCTCCCTGC TCCCCCGAGC CCAGCCCAGT CTGAGGTCCA TCCCCCTGTG AGGGGAGCTG 900
AGCAGTGCTG CAAACTCAGT GCTCCTGAGT ACCCTGGGGA TTTGCTGAAC TGCACATTCT 960
CATTCTGTAA ACCGGAGCTG AGCCTCTGCA CGTCTAACCT GCTCCCTGGC AATGCTGCTG 1020
TTACTGAGCA GAGTGGAAAA GTGCTAGACA ATACATTGGG GGGAAATTTC AGTCTCAAAT 1080
GCATTGGAGC AGAAACCAGA ACTCCCTGTC AAGCTGCTCT GTGGGTTTTT GAAGCGAAGT 1140
GTGTTGCTCT TCACTGGCTG CTCTGAGCTG CTCAGAGCGG 1180