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

TagContent
EnhancerAtlas ID
HS118-18537 
Organism
Homo sapiens 
Tissue/cell
Liver 
Coordinate
chr8:97304510-97305930 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs80260687chr897304689hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HLTFMA0109.1chr8:97304545-97304555AACCTTATAT+6.02
TFAP2AMA0003.3chr8:97304749-97304760TGCCTGAGGCT-6.32
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr89730461597304663
Number: 1             
IDChromosomeStartEnd
GH08I096293chr89730550097306614
Enhancer Sequence
CTGTCTCAAA AAAAAAAAAA AAAAAAAAGA AAAGAAACCT TATATTTAAA GTGCTATACA 60
TTGTAATATA TTGAAATAGT CACCCTAATT CTCAAAACAA TACAGTGTGA AAAAGACGTG 120
TCATAGATTC AAGGAAGCAC GATAGTTAAA AATGGTACAG TCTGTGTAGA GGTCCTGATT 180
GGGGGTGTGG GGAGCTGGGA CCAGTCTGAG CTGGGACCAG ATCATGAGGC AGAGGGCCCT 240
GCCTGAGGCT AGGAGGCTGC CAGGGCTGAG CCAGCTGGGA TGAGGAGTTT AGGTGTTATT 300
CTAAGTGTAT GAAAAGGCCA TGGAAGGTTT ATAAGCAGAG GAGCTACATG ACCTGTGTTG 360
ATGTTTTAGG AGGTCAATCA ATAAATACCT CCATTTCTAG TTGAGTTTGG AAACAGAAAC 420
AAGAGTTCAA AATCTCAGCT GATTTCTTCC TGTGAAAGCT CAGTGGAGCA GATTGCTTTA 480
GACCTGGGCT GAATTAAGCA AGCCTGTCTT CCCCTAGCCC ATTAGACAAC CACAAGCTGC 540
TTCTGCAAAG CAGGGCCTGA CCCACAAAAA TTGCTGCATG GCTGGGGGAG CTGATGAGAA 600
CCTGTGCTGT CTGTAAGCAA ATAATTTCCA AAGAGGACCC AAAAGAGGTT GGATCTCTTT 660
CTTCTTCCAA AGTCAGCAAC TGCCCCAGAG AGGAGTGAAG AGATAGTTGG GCTGGAGACC 720
TGGCGTGTGT AGTAGTGGAG ATCCTTCTAC ATTGGGACGG GCATGCTACC CAACCCCTTT 780
CTTCCCACCT CCTGCCCCAG ACACCCTTAC ACACATGCAT GCACGTTCCG TGATCTGATT 840
ATGATTTTCA AGATCTCTCT GTAGTCGTAA GCTAGATGTG AATACCTAGG TGCTTATTAT 900
AGCATCATCT ATACTTTGTT ATATGCCTGA CACATTCCAC AGTTTTCAAA AGCTATTATT 960
ATGGAAGTCT AAGCAAGAAA TAATAGTGGC AGCGAGATGC ATAAAAGAAC AACCTGGGGA 1020
GGTAAAGTGA ATAGGACTTG GTATTTGGTT AGGTGTCCAG CAAGCAAGGC AGAGGGTAAG 1080
GCCGCCAAGA TCAGCCTAGG ACCAGTTGGG AAGTCAGCAG AATCTGTCTT TACCCATCTT 1140
TTGCTCACAG GCATGCACCT GTCCACTTGA CCCCCTTTCC AGGCTTCAGC TCTACACTGT 1200
CTTCAGTTAA AGCCTGTTCC TCCTGGTTCC CAGGGTTCTG CCTGCATGCA GCTCTCTGGC 1260
TGCTTTAAAC TGCAATGCCC TGTGGCCCTT CCAGGACAAG GACCTCAGGT CTTATGAGGG 1320
GATAATTGGC AAATCTGTTC ATTACTAACT ATACTGCAAA TAGACGGATT GGTCTTTATG 1380
ATTTTTAAAA TGCCTTTCCG CATGTCAAAG CATAGAGCTA 1420