EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS108-06250 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr10:100140280-100141150 
TF binding sites/motifs
Number: 12             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Atoh1MA0461.2chr10:100140315-100140325AACATATGTT+6.02
Atoh1MA0461.2chr10:100140315-100140325AACATATGTT-6.02
LHX6MA0658.1chr10:100141046-100141056ACTAATTAGC+6.02
MAFFMA0495.3chr10:100140682-100140697TTGCAGAGTCAGCAC-6.42
MAFFMA0495.3chr10:100140682-100140697TTGCAGAGTCAGCAC+6.44
MAFGMA0659.1chr10:100140679-100140700GATTTGCAGAGTCAGCACTTT+7.51
MAFGMA0659.1chr10:100140679-100140700GATTTGCAGAGTCAGCACTTT-7.86
MAFKMA0496.2chr10:100140680-100140699ATTTGCAGAGTCAGCACTT-7.19
MAFKMA0496.2chr10:100140680-100140699ATTTGCAGAGTCAGCACTT+7.77
MafbMA0117.2chr10:100140688-100140700AGTCAGCACTTT-6.32
MecomMA0029.1chr10:100140781-100140795CCTTATCTTGTCTC-6.17
ZNF263MA0528.1chr10:100140897-100140918CCTCTCTCCCTGGCCTCCTCC-6.45
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr10100140570100140944
Number: 1             
IDChromosomeStartEnd
GH10I098380chr10100140135100141024
Enhancer Sequence
AATAACTTGG TAATTGTCAC CTGCCTTGCA AATTGAACAT ATGTTAGAAA GATGCACGCT 60
CACAAGCCCA CAGCCGGCTT GGTCAGCCAC ATCTGTCATT CCTCCCACCA GGAAGGCCAA 120
ATTCCTCCCA GAGCTGTAAA CCTCACATCT CACTGAGTCT CTGGACACCA TCACCCAGGG 180
GCTGTGAGAT CAGGAGGGCC TGCTGGTAAC TACTTAAGCA GCTGAGGTTC CAGTGCACTT 240
CAGGGTTTTA CAGGACTATG CCTCGAAGGA AGTGTTCCCT GCTGCTCTGG GGAAACAGGC 300
AATTGTAAAT CAGGTAACAA TGAGGCCCTG ACTTATTTAT CCTTCTAAAA GTTTTACATA 360
TTAGGGCCAG CAAGGGACAC ATTTGTCCAG TTCATGGCTG ATTTGCAGAG TCAGCACTTT 420
GGTAAGACCA GCCCGCCTTG CTCAGCAGGG TCGGCATGTG CTGGGGGCTT GGAGGAACCA 480
AGGCACCCTG TAGTGCTGAG GCCTTATCTT GTCTCTCGGT CTGGACTAAA TGTTATCTTT 540
CAGAGACATG AGACACAGGA TGGGAAGTCA CCAAACAGTG GGAAATTCTT CCTCTTGGTG 600
CTAAAGGTGC TTTTTCCCCT CTCTCCCTGG CCTCCTCCAA GTTCCTCCTC CTTTACAGGG 660
AACATTTGCC TGGAGAACAG CTGCACCCTT GTGATCCCAG AAATGACAGG GAACCATTAA 720
AACAGGAACA GCAGTGATAA AAGAAGTTTT CGGGCCTTTG GCTTATACTA ATTAGCAATC 780
AAGGCCAAAG CTGAACCCAA TGTCCCATAA TAAATTATGA CACATCCTTA CAAGAGAATA 840
TTAGGCAGCT ATTAAAAATA ATGTTTTCAA 870