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

TagContent
EnhancerAtlas ID
HS105-39559 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr19:18576820-18579770 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr19:18578257-18578272CAAGGCCAAAGTCCA+6.86
Hnf4aMA0114.3chr19:18578258-18578274AAGGCCAAAGTCCATT+6.24
PLAG1MA0163.1chr19:18577660-18577674CCCCCTTGGCACCC-6.22
RREB1MA0073.1chr19:18578427-18578447CCCCACCACACAACCACACA+6.16
RREB1MA0073.1chr19:18578992-18579012CCACAACCCACACAAACACA+6.16
RREB1MA0073.1chr19:18578611-18578631CCCCCACACACACAAACACA+6.17
RREB1MA0073.1chr19:18578580-18578600CCCACACACAACCCCCCACA+6.42
RREB1MA0073.1chr19:18578429-18578449CCACCACACAACCACACACA+7.27
Number of super-enhancer constituents: 20             
IDCoordinateTissue/cell
SE_01013chr19:18576872-18578784Adrenal_Gland
SE_04099chr19:18574803-18578345Brain_Anterior_Caudate
SE_06012chr19:18574448-18581892Brain_Hippocampus_Middle
SE_08139chr19:18574722-18578418Brain_Inferior_Temporal_Lobe
SE_08139chr19:18578435-18579400Brain_Inferior_Temporal_Lobe
SE_19379chr19:18578494-18579151CD4p_CD25-_Il17p_PMAstim_Th17
SE_26932chr19:18577284-18578376Esophagus
SE_31681chr19:18574807-18577161Gastric
SE_31681chr19:18578821-18579681Gastric
SE_41123chr19:18574701-18578554Left_Ventricle
SE_41560chr19:18575166-18581753LNCaP
SE_42344chr19:18574698-18579565Lung
SE_47511chr19:18577544-18578328Pancreas
SE_47511chr19:18578688-18581262Pancreas
SE_48120chr19:18574693-18581465Psoas_Muscle
SE_48694chr19:18574865-18577475Right_Atrium
SE_50125chr19:18574705-18578535Sigmoid_Colon
SE_51145chr19:18574427-18581554Skeletal_Muscle
SE_52434chr19:18574749-18577281Small_Intestine
SE_52434chr19:18577618-18578419Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 5             
ChromosomeStartEnd
chr191857881318578923
chr191857864218578703
chr191857944818579643
chr191857773918578633
chr191857896618579053
Number: 2             
IDChromosomeStartEnd
GH19I018464chr191857485118578411
GH19I018468chr191857914418581717
Enhancer Sequence
CTCACAACAG GAATGTGCTG GCCCTTTTCC CTAAAACACA CCCCTGCTCT TCAGCCAGTG 60
ACGGGACAGG CAGCCCATCC TCAGCAACAC ACACTGCGTA GAGAGGGGAC TCAGGCACCT 120
ATGCGGGTGG GCATGGGGCC AGGGGCCGTT TTCAGCAGCA ACAGCACTGC TGTCTGAGGA 180
CAGTGCTCAG CACCTGCCCA GATGCAGGGC CCCCACCCCA ATCGTGTGAC CCCTGGAAAG 240
TGGTTTGTCT GGACCATGAC TCACTTTCCC CACCACCAAA TGGACAGACC TGGCCTGCGA 300
CACCCTATGA GGTAAAATGC AACAAGAGGG GCTTGGGCAG CCACGCGCAA CTCTGGCGCC 360
CCTCCTTGGC GACCCCCTCT CAGCATCCCC CCACAAAGGA CATGGACTCC ACGTGAGTCT 420
CCATTTGCTG CAGCTGTGAA TCAGGTAGGC TTGTGTCCCA GGGGCTCACA GATCAGAAGC 480
ACTGGCCCCC AACAAGCCTG TCATGGGTCA CACCAGCCTG ACTTTGGCTG TGCCCCTGCA 540
GCCCAGCTGG GCAAAGCTCC AGCCCTGTCT GGGAGGACGG ACAGCCAGGG GCAGGCAGGC 600
GGATGGACGG ACTGCGCTGG TCCCGGCCAG GCTCAGTGCA GGGCGGCATC ACATCAGAGG 660
CCATTGCATT CCAGGCTGAC CCCAGACCCT CTGTCAACAG AGTTGGCCCT TCCTAAACTA 720
ATGCCTGGGC TTTGGCATGA GCTCCTCACA GTTAGACTGA CACATGAAGG GCGCTCAAAT 780
AGTCCACAAG GAGGGGACAA CATGGGGGGA GCCCTCAGGT CTTGTCCCCT GGCTGCAGCA 840
CCCCCTTGGC ACCCAAGCCC CGTCTCCTCC TCTGTGACAC CATGAGCGCG GGAGAGACTG 900
TGGCTGAATC TCCTGCCCCC TCGCCCCTGC TGAGCTGCCT CATACGCCCA TGGGAGGCTT 960
TGCCTGCCTG TGCCTCACCT GTGAGACAGG ACGGGGCTCC TGCCACCAGA CACGTGGAGG 1020
AGCACCAATC CCCGGCCCTG CTGTGTGGCC TTGACTGGGA CTTGTCCCCT GGGGTAGTGT 1080
TTGGACACAC AAGGGAAGCC ATGGCTGCAC CCAGCCCAGT GCCAGTCCCT GCTCCCAAGA 1140
CAAGAACAGT TCCTGGGTTC GGCCACTTGG GGCAGGAAGA GTCTGGTCTG GGCTTGCAGG 1200
CAGTCCCTGT ACCAGCCAGT CTGCCCGGCC TGCAGACCCT TCTCCAGAGG CCCATCCTGC 1260
CCCTTCCCCA GGCTGAACAC TGCCCCAGGA AAAAAGCCGT CCCATCTGCT GGGGTCTGCC 1320
CAGCATCCCC TCTCAGCCTC GAACATGTCC CCCTAAGGCA GGTGCCCTTG TCCCTGTCAT 1380
GCTGATACAG AAACACAAGC TGAGGGGTCA GGGCCCAAAC AGCGTGCTGG TGGAGGGCAA 1440
GGCCAAAGTC CATTGTGGGC CCACCATGCC AGGCCACACC TGAACACAAA CACACATCTC 1500
TATCAGGGTC AGAGAAGGCA GAAACGGCCT GCACTCAGCA TCGGAGAAAT CACACACATA 1560
TAGCCTCTGA TGATTCACCC TCGGACAGAG AAACCCTCCC CACCCGCCCC CACCACACAA 1620
CCACACACAC ACACACACAC ACACACACAC ACACACACAC ACAAACACAA CCCCTCCACA 1680
CACAATCTCC CCACACACAA TCCCCCACAA CCACACAATC CCCACACACA CACAAACACA 1740
ACCCCTCCAC ACACAATCTC CCCACACACA ACCCCCCACA ACCACACAAT CCCCCCACAC 1800
ACACAAACAC AACCCCTCCA CACACGATCT CCCTACACAC AACCCCCCAC AACCACACAA 1860
TCCCCCCCAC ACACAAACAC AACCCCTCCA TACACAATCT CCCCACACAC AACCATACAC 1920
ACACAATACC CAACACATAG CGCCACACAT ACAACCACCC CGACAGCACC ACACACAACC 1980
TCCCCCACAC ACAAACACAA CCCACACACA CAACCCACAC ATGCACAACC CCCACACACA 2040
CAGCCACACA CAAACCCCTC CACACCAAAC CCCTCCACAC ACAAACCCCT ACACACAACC 2100
ACACAAACAC AACCCAGACA TAAACCCCCA CACAGCCACA CAAACACAAC TCACACATAA 2160
CCACACACAC AACCACAACC CACACAAACA CAACCCCCAC ACACACAAAC AATCCATACA 2220
CACACACACA CACAAACACA ATCCATACAC ACAGAAACAC AACCTCCCAC ACACAAACAA 2280
CCACACACGC CCTGAAGCCT CAGCCAGAGC CATGTGGGTG ACCCTGGCCA TCCAGATCTG 2340
TCCTGCTTCG ACGCCACTGA GGTGTTTTTT CACCCAACAC ACACAGGTGC CACCCTGCCC 2400
TGCCTGCACC TCCCTTCCCA GATGTGACTT TTATTCTCGT TCATACAAGA AACTGGAAAC 2460
ACGCTGCTGG GATGAGGGAA GCTCAAGTTT GTGAGAGGCT CTGTGGTGGC CAGGTGCACA 2520
GGTGACATGG TGACCCAGAA TGAGCCAGCC AGGGAAGCTG GGGACCACAC GTCCAGGGAA 2580
ACCAAAAAGA GTGGCTGTGG GAACCTGAGC CTGGCCTGGG TGGCTCTCCC GCCCTCCTCT 2640
GTCATCTCTT TAACCCCCAC TGCCCCCTGT GGTCCTGGCC TGAGGCCCAA GTTGCCAGTG 2700
GCTCCTGCCC CACAGTGACT AAGGGCTGGG CACCCTCACG TGCAGCCCTG TCCCAGGAAA 2760
ACCCCAGCTC CACCCAGGTT GGCAGGACTC ATTCTGTCAC CCTGGCTTCA GGGGAGATGC 2820
CACTCAGCAG AGAGCTGGCA GTGAGACCAG GCCACTGCCT GTGGCCTGGG GCAGCTGTAC 2880
ACCCAGTCAG CACTGACAGG GCCCCCCTGC CTGAGCCTGC CCAGCAACCT TGCTTCTCTG 2940
TGGGTAGGGG 2950