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

TagContent
EnhancerAtlas ID
HS182-19507 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr7:2089860-2091250 
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MEF2AMA0052.3chr7:2090537-2090549GCTATTTTTAGT-6.18
MEF2BMA0660.1chr7:2090537-2090549GCTATTTTTAGT-6.62
MEF2CMA0497.1chr7:2090536-2090551AGCTATTTTTAGTAG-6.15
SCRT1MA0743.1chr7:2089885-2089900TTCCACCTGTTGCAC-7.02
SCRT2MA0744.1chr7:2089887-2089900CCACCTGTTGCAC-7.52
TBX20MA0689.1chr7:2090202-2090213CTTCACACCTT-6.32
TBX21MA0690.1chr7:2090203-2090213TTCACACCTT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr720910062091236
Enhancer Sequence
CAGCATCTGC GGGCATCACC GCCCCTTCCA CCTGTTGCAC TCCTACGAGA GCTAAGCCAG 60
GTATGAGGCC AGACCAGAAA CCAGAGACCA GGATGGAACC TCACGCGCCT GCTGGAAGCA 120
GGGAATCCCC TAGCCAGTGC CTCAGACCCA TGTCCACACC CACACGGGCA GACGGAAGCA 180
CCAGGCTGAG GGTGGTGAGC CAGGGGGTTC CTGGGCCGCC TCCACTCTGG CTGGTGTCAG 240
GCTGTGGCTT GACCTTTCTG GCAGCTCCGT TGAAGCACCC ACAGAACCAT GGAGACCACA 300
AGCCAACAGT GGCCTATCAC CGGCCTGGAG AAAGTCCAGA CACTTCACAC CTTCTGACTG 360
AGGCCAGGGA CCTCTCCCAG GACCATGGAC ACAGGGACCC AGGCACCCAC CCAGACTGTG 420
GTGCAGGGAA CTTACAAGGC TCTTGGGTGT GCCGTGACAC CAAGGACAAC TGAAGGGGCA 480
GAGGCTGCGG AGGGAGCAGC CCAGTACCCC CGAGGGCGGC TCAGTCCTCA GCAGGCCCAC 540
CCACCTGTGC CTCACAGGCC AGGAGCAAAC ACACCTGTGC GGAACGGCCA GGTGAGGCTG 600
GCTGTCACCT TTAACATCTC TGAATGTCTC CAGGAGGGGC CTAGAGAGGG TTCAGACACC 660
ACCACCAGGA TGCTGCAGCT ATTTTTAGTA GAAAGACTCA AGAGGCTTCC TTGGCAGGGA 720
ACCATGCCTT TGAGCATGAC CATCAATTTT CACCTGCAGC TAACTTCCTT TCCTTTCAAG 780
ATCAAGGTTA TTCAAAGATT TGGATTTCTT CGAAACTGAG TTTAAAGAGA GCATGTTTCT 840
CTACCAAACA GGATAGGGGA TTTTAAAGCA CAAACAAGGA CAATGTCAGG CCAAAGCCTG 900
GGTAGGCAGG ACAAGGTTCC GGGCCTGGTC CCTCCAGCCC TTCCCAGACA CCCTGCAGGC 960
CCTGCTTGTG TCCCCCCGAG GCTGGGCTAA AGCCACCTGT GCCAGCTGGA TGATGCCTGG 1020
CCTGGGCACT GGAGGAGCCT CCCTGGGCTC CTCTCTAAGC CTCGGTCTCT CTGGTATAAA 1080
CCTCCAAAGC TGAGGGGGAC TGGGAATTCC ACAGCCTCTC TCCTAGCAGG ACACTCCAGG 1140
TTTCTCGTCC ATAACCCACG TGGTGCTGTG GAGCCTTGGC CTACAGGACA GAAGGGGCTC 1200
CTGGGATCTG GATGAAGTGG TGGCGAGGGG GGCGCTGACC TTGTCCTTCA GGAAGAGCCA 1260
CGTGGCTCAG CAGGCAAGAT CCAAGACGTT TCAACGTGGT ATGTTAGAAA CTCACACTTA 1320
ATGCAGAAAA GCCCAGGAAC GAGACATTGA AACCGCACAT GAAGACTGGG CCTTCCCTGC 1380
ATCCGCCGGG 1390