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

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EnhancerAtlas ID
HS056-00214 
Organism
Homo sapiens 
Tissue/cell
GC_B_cell 
Coordinate
chr1:20496900-20498390 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
MAXMA0058.3chr1:20497856-20497866ACCACGTGCT+6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12049775520498287
Number: 1             
IDChromosomeStartEnd
GH01I020171chr12049769620498750
Enhancer Sequence
GGAGTTTCCA CAAGACTGTG AATGCCAGAA GAGCAGGGAC TGGGTCTGCT TTATTCTGTG 60
CCCCTGGCCC CTGGCACAGC ACCGGCACTG GGCGGGTACC CAGTGGATGC TCGCTCAATA 120
CTGGGGCAAG TAAACCAATG GGCCTGGGGC TCAGCACATG TCAGCAGCAG ACTCTGGATT 180
AGAACCCAGA TCACCTCGCT CTCAGCCCTG CTCCTGGGGG CAGGGGCTTG GCAAGGTGGG 240
GGTGGGGATG ACAGGGGCTG GCCTGGTCCT CACGGGCTGG GTCAGCTGAG GAGGCGGGTG 300
CTGATGCCCT GGTACTGATG CGGAAGCCTC CTCCCACGCT AGTGCCCTGA GCAAGGCTCT 360
GGACTCAGGA GCCCTGGTCA AGGCTTCAGG AGCAACTGGC TGCTTCTGCT CTGAAGGGGC 420
AACGTGGGAA GAAAGTACAG CCCAGGCCAC GTACTTTCGG GTCCAACTCC CAGCCCTGGC 480
TGGCACCTCC CACCACTGCC CAGCAGTGCC ACTGCCTGGG GCTCCAGCCT CTGCTCCTCA 540
ACCTTTGCTC CACTCTCCCT CATCTCCTGG GGTCCTGGGC TGGGAGGGTG AAGAGCATTG 600
AATAGAGAAG CTTCCCTGGG TGCAGAGAGC CTAGGCCAGC CCTGGCGAGT GCAGCCAGCC 660
CACAGGAGCC CAGGGTGGAG GCTTGGGCTG GGCCAGCCAG GTGTCCCCAC CCCTGTGGCA 720
AAGACAGGTG GGAAGAGGCC ATGGGAAACT CGATCCCTGG AGGCCACCTT CTCCAGTCCC 780
CTCTCCCCAT CCCTCCCACC AGGCCCTGAT CCCTTCCCCT CTCCTGAACA TGGCCTTGGA 840
GGTGTCACAG AAAAGACACT TTGCTTTAGG CCTGAGAAGG ACCACACCAG AGAGCTCCAA 900
CTCAGGAAGT CTCCTTGAGC TCACGTGGGG AACAAAAGGG GGTTCTTTCC CTGTCAACCA 960
CGTGCTGGTG GCAGTGGGCA GGGCAGGCCA AGAGCTGAGG CAGGTCCTCC CGGTGCAGGG 1020
GTCCGAGCCC CCAACCCACA CAGCTGGTGC CAGGGAGACC TCACAGTCCT AACTCTGGGT 1080
ATTGGTGTGT GCTGAGCTGA AGTGGTGGGT TGGGGGAGCT CAGGAGACCA GGGTTCTGAG 1140
CCCTGGAACC CACTACGGGA TGGAGGATGT ATCTCCCGCC ATAGGGGATG AGTGGCAGAG 1200
AGGTGGTAGT TCCCTGACCT CAGGAGGAAA CAGAGGAACT CCAAGGTGCA CTCACAGCTC 1260
TGAATAAATA CACCTGGGAA GGAAAGTGAT TCATGCAACC CCACGAGGCC AGGCAGGAAG 1320
TGAGCCACAC ACTATAAGAA GCCACTTCTT CTTTTTTTTT TTTTTTTTTT TTGAGACGGA 1380
GTCTCGCTCT GTGGCCCAGG CGGGAGTGCA GTGGCGCAAT CTCGGCTCAC TGCAAGCTCC 1440
GCCTCCCGGG TTCACGCCAT TCTCCTGCCT CAGCCTCCCG AGTAGCTGGG 1490