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

TagContent
EnhancerAtlas ID
HS059-00851 
Organism
Homo sapiens 
Tissue/cell
GM12878 
Coordinate
chr1:26845810-26847200 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr1:26847153-26847171GGAAGGAAGGAAGTCTGT+6.11
EWSR1-FLI1MA0149.1chr1:26847149-26847167GGAGGGAAGGAAGGAAGT+8.4
EsrrgMA0643.1chr1:26846555-26846565ATGACCTTGA-6.02
Nkx2-5(var.2)MA0503.1chr1:26845988-26845999AGGCACTCAAG+6.14
RORAMA0071.1chr1:26846556-26846566TGACCTTGAT-6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12684601726846210
Enhancer Sequence
CTTCTCTAGT ACATTTCATT CAAACAGATG GCTGCTACTT CTCTATTGTC ATTAATCTTT 60
TCATCATCTT CTTATTCTTC TTAGCACAGT TGGGGCATAA CATATTATCT TCTGTGCCTG 120
GGGATGGGAA AATGCAGGCA GGTAACAAGA AGAGAGAAAT CATCCTCCTG TGAGTGGTAG 180
GCACTCAAGC CTGACCTGCA TGAAACTGCA GGCGTACTCA ACCCTTTGTG TCTGCCGAGA 240
GAAGTCTGCC ATGGACCACA CACCACCTGA CACCAGCGGC TTGCATCAAA AAGGCCTCAA 300
GAGAAACAGG AATGGAACTT GAATTCACAG CCTCAGGCTC AACAGCTCTT GCAGCAATTC 360
TTGCCCTTGA TGCCAACATG GCTCCCTGCG CTGAAGTTAT CACTTCGACT GTATTCGTCT 420
CTTCTGCTCT CTCATTCATC TCATAAGTTT TCTGAAGCCT TGCTCTCTTG GTCACTGCCT 480
TGTGTTTCCT TGAACACCGC TGTAATCTGG TCTCTTGTGA CATTTCAGGC ATATCTTGCT 540
GTTGTTCAGG GTAAGCAGGC CTATGGACCC TCAGATAAAC TTCGATTTTC TTGCCATTAG 600
TACTCAAACT GAGTTGTTGG CACCAGTCCC GCAAAGTGTC CCAACACACC TTATTAATGG 660
GAGGCAAAAT GGTCGGCAAG GGAAGAGCTG GTATTTTGCA TCTAGCTTTT TGTGGAGCTG 720
TAAATTGTTA ATTTGTTTGA AGTAGATGAC CTTGATTGTA TTTCATAGGT TTCTCCAGTT 780
TGACATCAGA AGTTGAAGAA ACACTTGGTT CTGTTTGTTC CATATTTGGG TCATCTTTAA 840
CTGGCAGCAA TGTCAAAATC ACACTTTCCT CATCAGCTAC TTCCCCCTCA AAGAAATTCT 900
TCTTGCTGCT ATCCAAATTT GAGTCTGACA TTTTCAGCAA CACCCCTGTC TTGTCCATTC 960
GGTGATACAT TTTTTTTAAA ATTAGGCCTG GCATGATGGC TCATGCCTGT AATCCCAGCG 1020
CTCTGGGAGG CTCAGGCAGG CAGATCACTT GAGTCCAGGA GTTCGAGATC AGCCTGGGAA 1080
ACATGGTGAG ACCCCAGTCT CTGGGACTAC AGGCGTGCAC CACCACACCT GGCTAATTTT 1140
GTATTTTTAG TAGAGACGGG TTTCACCAGG CTTGACCACT CCCTCTTTGG CTTCGTTCTC 1200
ATTCATCCCC TGACCACAGT CAGGGGAGTC CCTCCAGGCT GAGGCCTCAT GTCTTCGCTG 1260
CACACAAGTG CAGAACCCAC TCAGTGAACC CCAGGCCCCA ATCTCTGGCT CTCTCCCTTC 1320
TTTGCAGGGG GAAGAATTTG GAGGGAAGGA AGGAAGTCTG TGATTGTCAC CTACCATTTA 1380
TTTTCTTCTT 1390