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

TagContent
EnhancerAtlas ID
HS012-15697 
Organism
Homo sapiens 
Tissue/cell
Caco-2 
Coordinate
chr19:48994800-48996950 
Target genes
Number: 40             
NameEnsembl ID
PLA2G4CENSG00000105499
LIG1ENSG00000105486
C19orf68ENSG00000185453
CARD8ENSG00000105483
ZNF114ENSG00000178150
CCDC114ENSG00000105479
CTCENSG00000248146
EMP3ENSG00000142227
TMEM143ENSG00000161558
SYNGR4ENSG00000105467
KDELR1ENSG00000105438
GRIN2DENSG00000105464
GRWD1ENSG00000105447
KCNJ14ENSG00000182324
CYTH2ENSG00000105443
LMTK3ENSG00000142235
SULT2B1ENSG00000088002
SPACA4ENSG00000177202
FAM83EENSG00000105523
SPHK2ENSG00000063176
RPL18ENSG00000063177
DBPENSG00000105516
AC008888.7ENSG00000232871
CA11ENSG00000063180
NTN5ENSG00000142233
FUT2ENSG00000176920
MAMSTRENSG00000176909
RASIP1ENSG00000105538
FUT1ENSG00000174951
BCAT2ENSG00000105552
HSD17B14ENSG00000087076
PLEKHA4ENSG00000105559
PPP1R15AENSG00000087074
TULP2ENSG00000104804
NUCB1ENSG00000104805
BAXENSG00000087088
FTLENSG00000087086
GYS1ENSG00000104812
RUVBL2ENSG00000183207
SNRNP70ENSG00000104852
TF binding sites/motifs
Number: 19             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF16MA0741.1chr19:48996445-48996456GCCCCGCCCCC+6.02
KLF16MA0741.1chr19:48996104-48996115ACCACGCCCCC+6.14
KLF5MA0599.1chr19:48996445-48996455GCCCCGCCCC+6.02
KLF5MA0599.1chr19:48996526-48996536GCCCCGCCCC+6.02
KLF5MA0599.1chr19:48996612-48996622GCCCCGCCCC+6.02
KLF5MA0599.1chr19:48996633-48996643GCCCCGCCCC+6.02
KLF5MA0599.1chr19:48996645-48996655GCCCCGCCCC+6.02
KLF5MA0599.1chr19:48996778-48996788GCCCCGCCCC+6.02
KLF5MA0599.1chr19:48996811-48996821GCCCCGCCCC+6.02
Klf12MA0742.1chr19:48996744-48996759GGCCACGCCCCACTC+6.02
Nr2f6(var.2)MA0728.1chr19:48995662-48995677CGAACTCTTGACCTC-6.24
SP1MA0079.4chr19:48996442-48996457CAGGCCCCGCCCCCG+6.11
SP1MA0079.4chr19:48996101-48996116TAGACCACGCCCCCG+6.29
SP2MA0516.2chr19:48996229-48996246CCTAGTCCCGCCCCATT+6.08
SP4MA0685.1chr19:48996742-48996759CAGGCCACGCCCCACTC+6.08
SP4MA0685.1chr19:48996101-48996118TAGACCACGCCCCCGTC+6.33
SP4MA0685.1chr19:48996442-48996459CAGGCCCCGCCCCCGCT+6.35
ZfxMA0146.2chr19:48995687-48995701CCCGCCTCGGCCTC+6.01
ZfxMA0146.2chr19:48996442-48996456CAGGCCCCGCCCCC-6.19
Number of super-enhancer constituents: 3             
IDCoordinateTissue/cell
SE_34585chr19:48994657-48998131HCT-116
SE_65829chr19:48992785-48995418Pancreatic_islets
SE_65829chr19:48995676-48998227Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr194899500048996200
Number: 1             
IDChromosomeStartEnd
GH19I048489chr194899292948998057
Enhancer Sequence
GAAGGCAGAT TAGGGGGAAG CCAGAGGGGA CAAACCTTCA CGTCCCATTT ACCGCATCCC 60
CCAAAAGCAA CAAAACCGGC TAATATTTCT GGGGCTCTAG GAATCCCAAT TTGTAATCAC 120
TGACTCGCAC GCTCTGGAGA GGTGGCTGGA GCCCCTAATC TGGCTTCGAA GCCTTGGGCC 180
AGCCTTAACC TCAACCTGGC CAGAGGCTCC TTTCCTGACA GCGGAGCCCC GCGCACAGCT 240
AAGTAGCCCA ACGCAGGGAT TCTCTCCTGG CTCATTAACG TGAGGCCTCC ACCGGATCCC 300
CTAACCCAAA GCGATCTCCA TAAGCCCCAC CCCGTCCACG TCAGTCCCAC CCACCTCTGA 360
GATCTTGACC TGCTCCAGTG GCCCTCCCAA CCCCTGCCCC ATCCTGAGCG CATGCCGTGC 420
TGGATGCTGT GACCCTGCCC CTGAGCCCTC CCTCAGAAGT AGACCTGCTC CCGCCCTCCA 480
AGTCCCACCC CTCTGAAAAC ATTTCAGTGG CCCAGGCCCC AGTTCTTGGC CTTGTTTCCA 540
TTCCTTTCAT AATCTCAGCC CAGTATGCCC GCCCCAGGTT CATCTAGACA AGGTCCCAGT 600
TCCTCAGCAC CACTCGCCCT CCCTTTTTCT CTTCAACACC ATATCCTGTG TTTTTCTTTT 660
TGTTTTAGAC AGAGTCTCAC TGTCGCCCAG GCTGGAGAGC AGTGTTGTGA TCATGGCTCA 720
ATGCAGCCTC AACCTCCTGG GCTCAAGCGA TCCTCCCACC TGAGCCTCCT AAGTAGCTGG 780
GACTACAGAT GCGCACCACC ACACCAAGAT AATTTTTTTC TTTTTAAGAG ACGAGGTCTC 840
GCCATTTTGG CTAGGCTGGT CTCGAACTCT TGACCTCAAG TGATCCTCCC GCCTCGGCCT 900
CCCAAAGTGC TGGGATTACA GGCGTGAGCC ACCCGGGACA GGCCTAACTC TTAACACATT 960
CCTCAACCCA TCTCTCTAAA GACCCGTCCC AGTCGTTAGG TTCGCTCATC CCTGACCTCA 1020
CCCCAGAATA CGTTAAGACT GCCTGCTCCA TCTCTGAAGC CCACCTGCAG CCTAGCCATG 1080
GCCCTTCCCT AGTGGGTAAG ATCTGCTCCA ACCCGAACCA GCCTACAGAC ACTAGAACTC 1140
TAGTCAACAA ACCATGCCCA AACTCTCACT AGGCCCCTTC ACCATCCAGG CCTCTTCTCA 1200
ACACTTCCTC CCTAGCCTCT CCAGGATCCC ATACTTGACT ACCCAGTACC CCCTCTTTCC 1260
TTCCAGACCC ACACTCTCTC TCCAGACCTC TCCTCGCCCT CTAGACCACG CCCCCGTCAC 1320
AAGCCCTGCC CTCACCCTAG GTCCCGCCCC AGCTCTAGGC TCGGCCCATA CTCCTGGCCC 1380
TGCCCCATTG CCAGGCCCTG CCCTCACACT CAAAGCCTCC TCCCATCTTC CTAGTCCCGC 1440
CCCATTTCCC TGACCAGTCT CTCCCCAGAC CCCGCCTTCA CCCCTCAGGC CCTTCCCGCG 1500
CCCTGCTCCA TCCGCCCCGC CCTAGGCTCC GCCCCCATTC CAGCCTTGGA TTTTCTCCAG 1560
GCCTCCTCTT GCCGCGCCAC AGACTTGGCC TCCCTCAGGC CCGGATCCAG ACTCTGTCCC 1620
GATCCTAGGC GCGGTCTCCT TCCAGGCCCC GCCCCCGCTC TAGGCTCAGC CTGCCTTCAA 1680
ACCCTGCTGT AGACCCCGCC CCACCCTAAG CTCAGCCTTC GTCTAGGCCC CGCCCCAGGC 1740
CCTGCACCTC TAGGCTCGAC CTCCCTCCAG GCCCCGCCCT GGGCTCCGCC CCCCAGCCCG 1800
CCCTCTCCCT GGGCCCCGCC CCACTCTAGC TCGGCCCCGC CCCAGGCCCC GCCCCACTCT 1860
AGATTGGGGC TCCCCTTAGG TCCCACCCCA ATTCAGCTTG CCCTCCCTCC AGGCCCCGCA 1920
TCACTCCAGC TCGGCCTCCC TTCAGGCCAC GCCCCACTCT AACTCGGCCT CCCTCCAGGC 1980
CCCGCCCCAC CCTAGCTCGG CCTCCCTTCA GGCCCCGCCC CACTCCAGCT CCGCCTCCCT 2040
CCAGGCCCCG CCCAACTCTA AGCTCGGCCT CCCGCCAGGC CCTTCCCGGC TCTAGGCTCC 2100
TGCTCCCTCC AGGCCGCGAC CCCGAAACCG CGCCCTCTCG GGTTCCGCAC 2150