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

TagContent
EnhancerAtlas ID
HS091-39814 
Organism
Homo sapiens 
Tissue/cell
HepG2 
Coordinate
chr5:177640100-177641790 
Target genes
Number: 8             
NameEnsembl ID
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr5:177640763-177640784TTCTGGTTTCATTTTCCTGTC+6.29
IRF2MA0051.1chr5:177640762-177640780CTTCTGGTTTCATTTTCC-6.57
Nr5a2MA0505.1chr5:177640152-177640167CCTGGCCTTGGCCTC-6.13
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_23127chr5:177638094-177644087Colon_Crypt_1
SE_23791chr5:177639001-177643398Colon_Crypt_2
SE_24793chr5:177639486-177644175Colon_Crypt_3
SE_28105chr5:177630835-177643084Fetal_Intestine
SE_28930chr5:177630824-177643883Fetal_Intestine_Large
SE_50201chr5:177630779-177644241Sigmoid_Colon
SE_52441chr5:177630834-177644193Small_Intestine
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5177640767177641115
Enhancer Sequence
CAGCCTGTGA GGACAGGACA CCCCTTCACA TGGCCTTCAA GGCCTTCCTC AGCCTGGCCT 60
TGGCCTCATG TCCAGTGCTC CAGCCACACT GTCCTCAGAG CCTTCCATGG GCCAGTTCCT 120
GCCAGGTCAT TTTACTGGTC ACCTCTCCCA GAGTCCTGTG CATCTGGCCC ACAGCAGCCT 180
GCTTGGAGTG CACTGCACCT GGCCCTGAGC CTGCTGCCCC ACAGAACAGG CACCTTGCCT 240
CACCTAACCC TGGAGCCACA GTCCAAGCCA AGAATGAATG GCCACAGGGA AACGCCAGAC 300
TGCAAGAGTC ACCTGCATTC TCTGGTTTTC TGTGTGGTTT ACGTGATGTA TATTGTTTCC 360
TTATATAGAG AATGTCCAAC ATTGCAGTTG GTGTAATGAG CTCCACGTGC CCCTCACCAG 420
CTTCAGGCAT CTTCCTGCCC TGTCTTCCGG GTTATCTTAC AATTCCAGTT TAAAATGTCC 480
AATTATTCTT AGGAAGATGG CTTTATCTTA ACATCATTTG TAGCTAATAA TCACTTTTAG 540
TCCACAGTCT AACCTCATCT CTGAGATGAG GGGTCTGCAT GATTGTGTTT ATATTCTTTG 600
ATCATTGTTC CCCTTCTTTT GTAAACCTTG TTATTTTTAT TTCTTGGGGG TGGGGAGTGT 660
GCCTTCTGGT TTCATTTTCC TGTCCCAGTC TTCCTGGCAC TGACCATGGC CACGCCAGAA 720
AGAACAGGGC TTGGACTTTG GAGTTAGACG GCCCTGGGGC CAGATCTAGC TCTTGCCACC 780
TAGCAGGGTA ACTGCAGGTG ACTTACCCAT TTCCTCACTG AACTGGAAAA GCACCCCCAG 840
GGTATTGTGA GACACGGGCT GAACTTGGGA TCTGTTTCCT TCCATGCCAC CTGACCATTC 900
CGAATCCCTG AGGCTCCTGG GAGGGGGGTA GGAGTAAGCT GGGGATGTGA CTGACAGCAG 960
AGAGAAGGCG GGACCAGGAA AGGCCAAGTT CAAATACAGC ACAGAGATTT ACATCAATAC 1020
CACGCGTGTC TCACAATTTG AATAAGGACA CGTCAAATAC CAGAAGAGCT TTCCATGGTG 1080
GGCGTGGGGG AAGGGGTAGG CCTGGGGAAT GGAGATAAAA GGGAATAACA ATTCAACTAG 1140
AAGGAGAAGA AGTCCTGAGG ACTTGGGGTC CAAGTGAAAG GACAAGCAAA CCAGGGCATT 1200
GGGACCGGTG GAGTCTGAGT TCTGAGACAC CCCCGACCCA GCTTAGGAGC AGGAGTCTTG 1260
TCCATCCCAA CCACCTGTCG TGCGGCATGG GAACCCTGAG TCTAGTGCTG CCACAGCTCC 1320
CTGGTATGAA TAGAGAAGGT GTTTCCCTTC TCCAGGCCAA GGTGGCATTA GGGGTTCCTG 1380
GGTCTGAGTG CCCTGCTAGC TTGGGCATTC TAGGCAGAGG TGCTGCTCTG GTCTGGGAAT 1440
AGCCTGTGTC TCATCTGCAG CCTTTGTAGT CAGGCACTGG GTACAGAACT GCTAACACCA 1500
CTTATCTCTG TCCTCAGCTG ATAGGATCAG CTGTCCCCCA ACAACTGCCC CCACCCGCCA 1560
GCCCCAGCCC TCTTTCAATC AAGTCTGTGG CCCAGAGTGC TGGGGGTACA GATGAGGCTC 1620
CTTTCCACTG GCCCTGCAAA GAGGTACCTG TGGTGTCTCC TACTCCAGGA AGCAACTTGT 1680
TTCAAGAAGA 1690