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

TagContent
EnhancerAtlas ID
HS050-40864 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr2:242436090-242437030 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
BHLHE41MA0636.1chr2:242436700-242436710GTCACGTGAC+6.02
BHLHE41MA0636.1chr2:242436700-242436710GTCACGTGAC-6.02
MITFMA0620.2chr2:242436696-242436714CAGGGTCACGTGACTAAC+6.7
MITFMA0620.2chr2:242436696-242436714CAGGGTCACGTGACTAAC-6.7
USF1MA0093.2chr2:242436699-242436710GGTCACGTGAC-6.14
USF2MA0526.2chr2:242436698-242436714GGGTCACGTGACTAAC-6.21
USF2MA0526.2chr2:242436696-242436712CAGGGTCACGTGACTA+6.66
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2242436489242436845
Enhancer Sequence
GAAGTGAGGT GGCCCAAGGA AGCCTCTGCC CCTGCCCTGC CAACGGGGAC CCTAGTGGTC 60
CTTCCCCACA GCACCTACCT TCCCCCTACA CTCCGGGGAA TCTCGGACCT CGGTTCTCAG 120
GAGGGGACCA GATGGCTTCC TCCCAGCCGA GGGTCATGGA AGCCACTCAA TGGGTCTAAT 180
CAGACCCAAA AACACGAAGC CCAGAAACCC CCAAAGCACA CGGCACCGCC AGGCCCAGAT 240
CTGACCTCCA TCAGGACACC AGCATCTGAG CCTCCTGTCA CCGGGTGTCA CCCACCCTCG 300
GGGGGCTGTG GCTGGATCAG CAGGCTGCCC AGGACCTGGA CCCGAGTGGC TGCTTCCCGC 360
TGGGGCCTCC ACATGGGCTG GGGCCAACGT CCCTCGACCG TGCTCCTCCC TTTGCCGTCC 420
TCAGGCAGGC CCTGCCTTCA CCACCTCTCA CCCACATCCT CCATCCTCCC TCCCCAGGCT 480
CCAGGTGGGG CTCCTGGAGG GCACACCTGG GCCCAAGCCC GCTGGCCACG CCCTGGGCAC 540
ACAGATCCTG GCTGTATCAC ATTTCTGAGG ACGGTGCTGA CTGCCCATCA GCAGGTGACG 600
TTGATGCAGG GTCACGTGAC TAACCAGGGC GGCACCTGCC CGGGGATGGA CCCCGACTAA 660
ACCTTCTCTG CTTTCTCTAT AGAAGGATCA TCTGTGTTTG CACCTGAAGA AAAAAAAGTC 720
ACCCTAGGAA CCCAGAGAAC CTTGGCAGGT CTGGGAGTAC AAAAGGAGTC ATTGCAGCAG 780
ATTCTGCTCC TTCCACTCAG AAAACCCAGC CCACAATCAG CTGCAGGAAA GCTAGAAGCT 840
GAAACCACCC CACAGTGCTG TGAGGGAGAC ATCTCCGTGC AACAGTGTCA CAGCCTTGTC 900
CTTGACGGGA CTCCAGGCCC AGTCCCAGCC CCATCCTCAC 940