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

TagContent
EnhancerAtlas ID
HS118-19845 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr9:139531740-139533160 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr9:139531803-139531818GAGGTCAAGAGATCG+6
ZNF263MA0528.1chr9:139532885-139532906AGAGGAGGGGGAAGATGAGTG+6.4
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9139532061139532486
Enhancer Sequence
TGCAAATTAA AATTACAGTG AGATGCAGCC GGGCGCAGTG GGAGGCCGAA GCAGGCGGAT 60
CATGAGGTCA AGAGATCGAG ACCATCCTGG CCAACATGGT GAAACCCATC TCTAAAAATA 120
CAAAAATTAG CCGGGTGTGG TGGTGCGTGC TTGTAGTCCC AGCTACTAGG GAGGCTGAAG 180
CAGGAGAATC GCTTGAACCC AGGAGGTTCC CAGGTTGAAC CCAGCCTGGC AAAAGAGCAA 240
GACTCCATCT CAAAAAAAAA AAAAAAAAGA AAAATTACAG AGAGTTGCCG GTACATACCA 300
GTTCATCAAT GGTAGCAAAC ACATCTCACG AATGTAAGAC GTTAAATAAT CAGAGAAACT 360
GTGTGCAGGC TGTATGGAAC TGTCACGAGA CAACATTGCA ACAAATTCAA CTTAAAAATC 420
TTAATTGGCT TTCATTCACA ATTCTGAAAT TGGCTTAGAA CCAGGACAAA TTCAGACCTG 480
GAGCTGCACA ACGTTCATGG AAACGGAAGT GATGCGCAGA GGCAGTTTTG GTGGTGGCCG 540
CTGGGCACTT TGCCTTGAAA TCAGCGGCCA CTGGCAACTG ACAGCTGGCA GCTGCGGTGA 600
CCTGGACCCA GTCCCTGTGA CAAGAGGCCA GCCTTCTGTG GCCTTCAGGC CATGCCAGGC 660
TGCAGTTTGC TGTATGGACT CATGCCCCAG GCCTCCTCGG TGAAAACTTA ACAGGACTCT 720
CGGGTTCATT TTGAAACCTT TATGTAAGTC TTAGCCGGGC ACGGTGGCTC ATGCCTGTAA 780
TCCCAGCACT TTGGGAGGCT GAGGCAGGTG GATCATGACG TCAGGAGTTT GAGACTAGCC 840
TGACCAACAT GGTGAAACCC CGTCTCTACT AAAAGTACAA AAACTGGAGG CCGGGCACAG 900
TGGCACATGC TTGTAATCCC AGCTACTCGG GAGGCTGAGG CAGGAGAATC ACTTGAACCC 960
AGGAGATGGA GGTTGCAGTG AGCTGAGATC GCGCCATTGT ACTCCAGCCT GGGCAACAGA 1020
GCAAGACTCC ATCTCAGGAA AAAAAAAAAG AAGAGAAACC TTTATGTAAG TCTAAATCTA 1080
TTCTGAAATT AAAAGTTGAT GTAAAAATCT TTAAAACGTA GGCTGCAGTC ACATGGGGGG 1140
AAGCCAGAGG AGGGGGAAGA TGAGTGAAGC CCAGCTCTGC TCCTGGGAGC TGAAAGCACA 1200
GGTGTCAAAA CACCAGCCGG GAGTGCGGCA GTGCAAGGCC TGGCCCTGCC TTCCCCAAGT 1260
GCTCAGGACA GAATTTTCCA TCTGTTTTAT TTTTTAAATT TTTATTGATT GATTCATTCA 1320
TTCATTTATT GAGATGAAAT CTCGCCCTGT CGCCCAGGCT GGAGTGCAAT GGCATGATCT 1380
CGGCTCACTG CAACCTCCAC CTCCCGGGTT CAAGCAATTC 1420