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

TagContent
EnhancerAtlas ID
HS073-07777 
Organism
Homo sapiens 
Tissue/cell
GM19238 
Coordinate
chr19:45225020-45226240 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr19:45225175-45225190TGAACTCCTGACCTC-6.22
SPI1MA0080.4chr19:45225788-45225802CAAAAGGGGAAGTG+6.41
SPIBMA0081.2chr19:45225790-45225802AAAGGGGAAGTG+6.07
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_09606chr19:45225026-45227473CD14
SE_23877chr19:45225227-45225635Colon_Crypt_2
SE_31568chr19:45225186-45226205Gastric
SE_34750chr19:45225301-45226193HeLa
SE_53360chr19:45224892-45226462Spleen
SE_62704chr19:45221152-45271677Tonsil
SE_65330chr19:45224918-45226537Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr194522544145225906
chr194522527445226089
Number: 1             
IDChromosomeStartEnd
GH19I044721chr194522504145229949
Enhancer Sequence
CACTCAGCTC ACTGTAACCT CTGCCTCCGG GGTTCAAGTG ATTCTCCTAC CTCAGCCTCC 60
TGAGTAGCTG GGATTACAGG CATGCACTAC CACGCCAAGC TAATTTTTGT ATTTTTAGTA 120
GAGACGGGGT TTTGCCATGT TGGCCAGGCT GGTCTTGAAC TCCTGACCTC AGGTGATCCA 180
CCTGCCTCAG CCTCCCAAAG TGCTAGGATT GCAGGTGTGA GCCATCATGC CCGGCCCTGA 240
TTCAGGTTCT AACAGGATCC CTCTGGCCAT GAGGTGGAAA GAGACTGTTG GGGGCAGAAT 300
TGTAAAGCGA GGGACAAGAA GAGTCAGGGG TCTCCAAGCT TTGAGCCTGA GCCACTGCAA 360
GGATGAAGCT GCCATTTCTG AGGCCAGAAG GCTGCAGGCA GGGCTGGGTT GGAGATTGGA 420
ATGAAGATAG GTCTTGTTTG AGGCCAATGA GGAGGGAGCC TCACCCGAGG CACACAGGCT 480
CCAGGCGGGA AGTTGGCGAC AAGTTGTGGA CTGTGGTTTT CACCCACCTC ATGGGGCCCC 540
CTCATCCTCT CCCCCAACTT CCCCTCACGC CGTGGTGGAG CCAGCTTTGT TTGTTTCCCC 600
CCCATCATCC GTTTCATGAT GGGGAAGACT GGTTTTCCCC TAACCCAACA GACACCTCTT 660
CCCTCAGCCT GTCCCTGACC CTCCCACCTC GGGAAGCCCC GAGCGGGCCT CCCAGAATGT 720
CCCGGCAGGA AGGGGCTGCT GCTACCGTTC ATCCAGCCAG ATGAACCCCA AAAGGGGAAG 780
TGGGTCACCC GTAGTCACCC GGCTCATGGT CAGCTCGGGA CTTCAGGATC TCGTCTCTTC 840
ACTGCACCCA CCACAGCCCT GGGAGGTTTT CCATGCACGC TTCTCATTCT CCCCACATTT 900
CACACGAGAA AACAGGGGCT CCAAGAGAGG CCCACACTCA CCTAAGGAGC TCGAAAGATA 960
GGGGCATCTG GATTTGAACC CAGGTCCTAG CAGATGTTGT TAGCTCAGAG GAGAAGGCAG 1020
AGAGGGTGAA CAGAACCCAG CCTGCCCTCC CAGATCCAGT GGGAAGGCAG ACTTGTCCCC 1080
AGGTAATAAT AGCCCAGCAG TGTTCACAGC CTGGGATGGA GGAGCCCAGG AGGCTGCAGG 1140
AGCTCAGAGC GCATGCCTGA CCCAGCCTGG GGTCAAGGAG GGCTTCCTGG AGGAAGGGAC 1200
AGCTCATCTG ATACCTAGAG 1220