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

TagContent
EnhancerAtlas ID
HS101-36986 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr6:26550410-26551790 
Target genes
Number: 43             
NameEnsembl ID
TRIM38ENSG00000112343
HIST1H3AENSG00000198366
HIST1H4AENSG00000196176
HIST1H4BENSG00000124529
HIST1H3BENSG00000124693
HIST1H2ABENSG00000137259
HIST1H2BBENSG00000196226
U91328.2ENSG00000234816
HIST1H3CENSG00000196532
HIST1H1CENSG00000187837
HFEENSG00000010704
HIST1H4CENSG00000197061
HIST1H1TENSG00000187475
HIST1H2BCENSG00000180596
HIST1H2ACENSG00000180573
HIST1H1EENSG00000168298
HIST1H2BDENSG00000158373
RP1ENSG00000217159
HIST1H2BEENSG00000197697
HIST1H4DENSG00000188987
HIST1H1PS1ENSG00000216331
HIST1H2ADENSG00000196866
HIST1H3DENSG00000197409
HIST1H2BFENSG00000197846
HIST1H4EENSG00000198518
HIST1H2BGENSG00000187990
HIST1H2AEENSG00000168274
HIST1H3EENSG00000196966
HIST1H1DENSG00000124575
HIST1H3FENSG00000256316
HIST1H2BHENSG00000197459
HIST1H3GENSG00000256018
HIST1H2APS4ENSG00000218690
HIST1H2BIENSG00000168242
HIST1H4HENSG00000158406
BTN3A2ENSG00000186470
BTN2A2ENSG00000124508
BTN3A1ENSG00000026950
BTN2A3PENSG00000124549
BTN3A3ENSG00000111801
BTN2A1ENSG00000112763
HCG11ENSG00000228223
HMGN4ENSG00000182952
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF5MA0599.1chr6:26550823-26550833GCCCCGCCCC+6.02
ZfxMA0146.2chr6:26551645-26551659CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_14648chr6:26551567-26557745CD4_Memory_Primary_7pool
SE_30005chr6:26550514-26551441Fetal_Muscle
SE_35175chr6:26550328-26551599HeLa
SE_59570chr6:26550253-26578074Ly3
SE_61702chr6:26532165-26578026Toledo
SE_63024chr6:26532079-26573171Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr62655041826550804
chr62655090626551000
Number: 1             
IDChromosomeStartEnd
GH06I026549chr62655008426551428
Enhancer Sequence
CAGATATGGG GACATCTAGA CACTCCCAAG TCTGGGTCTG TTTAGTAAAC ATTATTAATT 60
TGTTCCCTTA ACCATAAACA TCTAGAGGCT AGGAATGCCT GACTTTCTGG GAATGCAGCC 120
CAGCAAAAGT CCCGGCCTCG TTTTCCTAGC CCTCACTCAA AATGGAGTCG CTCTGGTTCG 180
AATGCCTCTC ACAGAAATCC CGCTAAAATG TACCTCCCTC GGTTGCGGTG AGCCGTGATC 240
GTGCCACTGC ACTCCAGCCT GGGAGATAGA GTGAGAACTC CGTCTCAAAA AAAAAAAAAA 300
AAAATACCTC CTTCTTCTCT CAAAACTCTC CAATGGCTTC CACCCTGGGT CATCAACATG 360
GCCTGGAAGA GCCGTACTCT GGATACCCGA GGGCGCGGCC CCAGCGCCGC GACGCCCCGC 420
CCCTCTGGCT GCTCCGCTCT GGGATGCACT TCCGACGCCC TCTAGGCTTG GGAGTTCCGC 480
GCCTCTCGGT GTCGCCTGGG GGGCGTGCTC CGGTTGGCGC ACTGATTCCC AGTTGGGTAG 540
GGGAGGCTTG ACTGAGCTCC CACCCGGAAT TTCACCTTAG ACCTTTAAAG ACCTTGCTCC 600
GGCCTCCCGC GCCAGCGCTA ACACCTAGTC CTCTTTAGTG GAGTTCCGGC GGAAGGGGAT 660
GGCGGGCACC CGACGGTGGT CTCCTCCCAG ATGGCGAATT TCCGCGGCTT CTTCATCTTT 720
TAGCTCCCAG GGAGCCCTCT GGCCCCAGCA TGAAGCCCAT GGAGCCCTTT TCAAAATTGT 780
ATTTTTAAAA GCTTTTAAAA AATACACAGG ATTTTAAAGA AAGCCAATTG TACTACAAAA 840
CAGTTTTCAA ACGATTAAAA TAATTTCATA GAGTAATGTG TGCTTCTCAT TAATGCATTA 900
AATATTAAAC ATCAAGACCC GTCTTATGAC TGCTGTAATT TTCAAACAGT TGTCTTGGGT 960
ATTTGTAACA ACTGTATTGT GATACAAAAA TATGTGATTT TTCTTTTCTT TTTTTTTAGA 1020
CAGAGTCTCC CTCTGTCGCC TAGGCTGGAG TGCAGTGGCG TGGTCTCTGC TCACTGCAAG 1080
CTCCGCCTCC CGGGTTCACG CCATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTACA 1140
GGTGCCCGCC ACCAATTTTG TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACCGTATTAG 1200
CCAGGATGGT CTTGATCTCC TGACCTGGTG ATCCGCCCGC CTCGGCCTCC CAAAGTGCTG 1260
GAATTACAGG CATGAGCCAC CACCCCCGGC CAAAAATATG TGATTTTTCT TGATGACAGA 1320
GTCGTAGTTA CTTCTCTTTC AATTGTGGTT TGTTACCTGT ATTAGTAAGT GAAAGATATG 1380