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

TagContent
EnhancerAtlas ID
HS095-17679 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr2:225306780-225308050 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
INSM1MA0155.1chr2:225307302-225307314CACCCCCTGACA-6.22
NFKB1MA0105.4chr2:225307158-225307171GGGGGAATCCCCG-6.36
NFKB1MA0105.4chr2:225307158-225307171GGGGGAATCCCCG+6.46
ZNF263MA0528.1chr2:225307477-225307498GGAGGAGGGGAGCGCGAAGGA+6.23
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2225307433225307612
Number: 1             
IDChromosomeStartEnd
GH02I224442chr2225306718225307917
Enhancer Sequence
TTTGAGCTCA AGGGACATGG ATTTGGGAGG AATTCAAAAT GTGAAGCCTA ACTCAGGATT 60
CAGGAACCAG ACTAACAGAG GGCAATGAAA CAAAACCAGA GAACTCAGGC CCAGAGCCAG 120
CGAGGGAGAG GAAGGACGCC GAAGCGTAGC GTCCCGCGCC GCCCCCCGCC AACCCGGGAG 180
GACGCAGACC CCCCAGAGCC GGTGTCCAGC CCCACCTCTC CGGGCGCCTG CAGGAGGGGA 240
ACCGCGCGTC CCATCGCCCG GACCCCGGGC CGGCGGCGCG GCCGAGTCCC GCTGCTTCCG 300
CACTCGCCCC GGGACCCGGA CCCCCGCCCC ACCGCGCCCC TCCACCTCCC CGCCGGCCGG 360
TGCCACGTGT AACGCCGCGG GGGAATCCCC GGGGACACAG GGCTGGCTGG ATTCGCCTCT 420
CGGCCACAGC TCTGCGCTCC ACGAGCTGCT CCTGCCCGGT CCCCGCAGGA CTCGAACCCG 480
CGACACCTCT GCCGCGCCCT AGCCCTCGCG CCCCGCCGGA GTCACCCCCT GACACTGCCA 540
GGATCCCCGC CCGGCTGCGG GCACCACGTC CCCCGGGCCT TCGCGGGGCC CCGAGGGCCA 600
AGACCGAGGA CGCGCCGAGC CGAGGCTGCC TGGGGACCTG GTCCATCCGG TTCTGATGGG 660
GTCCGCAGGG AAAAGGCACT ATCCCGGAAA GCTTCCTGGA GGAGGGGAGC GCGAAGGACG 720
AAACTGGGCC TCCCTCTAGG CGGAGCTTAG TGTTTAAAGC TGGCCGGCCT TTCTCCTTTT 780
CATAGTAATT ATTCTCTCAC TAAGCTCAGG AAGCACGCCC TCCACCATCT CATTAAGCGA 840
ACCGGCTGTG GCTGACTCTT CCCTCCTCTA ACAACTGTGG CTCCTCATAG CCGGCACAAT 900
GACGTCCAAA GCTGTCGGCT CCCGCACGGG TTCCTCCCTT TGAGGCTTGT CTTTCGCACT 960
CCTTCCACCT GCTCGGAGAA CTGCGCCCAG GTGGGTTCAG CAACTAGCAG GTGCCATGAA 1020
GAGACCCTCA GAGAAGCGGC CGGCCTACCT GGCGCCCGTT ACCCCTCTCG CCGCAAACCC 1080
ACTTCCCTGA ACTGTTTTGC AGTTCACAGC CTCTCTCCCC GCTCTAAAAA CTAAAAACAA 1140
ATGAACACTG AAGAGCTCCA GGCTTCATTT TTTTTTTTGA GACGGAGTCT GGCTCTGTCG 1200
CCCAGGCTGG AGTGCAGTGG CGCGATCTCG GCTCACTGCA AGCTCCGTCT CCCGGGTTCA 1260
CGCCATTTTC 1270