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

TagContent
EnhancerAtlas ID
HS086-06252 
Organism
Homo sapiens 
Tissue/cell
HEK293 
Coordinate
chr19:1453610-1455140 
Target genes
Number: 49             
NameEnsembl ID
WDR18ENSG00000065268
HCN2ENSG00000099822
FSTL3ENSG00000070404
PRSS57ENSG00000185198
PALMENSG00000099864
AC004449.6ENSG00000261204
ARID3AENSG00000116017
KISS1RENSG00000116014
R3HDM4ENSG00000198858
MED16ENSG00000175221
PTBP1ENSG00000011304
LPPR3ENSG00000129951
CFDENSG00000197766
SHC2ENSG00000129946
GRIN3BENSG00000116032
C19orf6ENSG00000182087
CNN2ENSG00000064666
ABCA7ENSG00000064687
HMHA1ENSG00000180448
POLR2EENSG00000099817
GPX4ENSG00000167468
SBNO2ENSG00000064932
STK11ENSG00000118046
C19orf26ENSG00000099625
ATP5DENSG00000099624
MIDNENSG00000167470
CIRBPENSG00000099622
C19orf24ENSG00000228300
MUM1ENSG00000160953
EFNA2ENSG00000099617
AC005330.1ENSG00000240846
NDUFS7ENSG00000115286
AC005329.7ENSG00000248015
GAMTENSG00000130005
DAZAP1ENSG00000071626
RPS15ENSG00000115268
APC2ENSG00000115266
C19orf25ENSG00000119559
PCSK4ENSG00000115257
REEP6ENSG00000115255
ADAMTSL5ENSG00000185761
PLK5ENSG00000185988
MEX3DENSG00000181588
MBD3ENSG00000071655
TCF3ENSG00000071564
ONECUT3ENSG00000205922
ATP8B3ENSG00000130270
REXO1ENSG00000079313
KLF16ENSG00000129911
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr19:1454017-1454036GGGCCAGCAGAGGGAGGCA+6.39
IRF1MA0050.2chr19:1454351-1454372AATTGCTTTCTCTTTTTTTTT+7.05
SP2MA0516.2chr19:1453716-1453733ACACGCCCCACCCACTT+6.18
SP8MA0747.1chr19:1453613-1453625AGTGGGCGTGGG-6.14
ZNF740MA0753.2chr19:1454982-1454995CCACCCCCCCCCC+6.44
Number of super-enhancer constituents: 4             
IDCoordinateTissue/cell
SE_04580chr19:1448784-1454146Brain_Anterior_Caudate
SE_07653chr19:1448648-1457040Brain_Hippocampus_Middle_150
SE_34483chr19:1453785-1454360HCT-116
SE_34483chr19:1454954-1456959HCT-116
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1914538731454140
Number: 2             
IDChromosomeStartEnd
GH19I001453chr1914536011454394
GH19I001454chr1914546611457763
Enhancer Sequence
GTGAGTGGGC GTGGGAACCC AGCCTCGGGC AGCTGGAGCA TGACTCGGTC CCCAGCGGGC 60
TCTGCCCTCT AATTCGCCCA CCCGCATATG TCTCTGCCCA CACCTCACAC GCCCCACCCA 120
CTTGCATATG GCACTGCCCA CCGAACAACC CCGCCCACCT CGGAGCTTCG TCCCCACGTG 180
GCCTCCCTCC CCCTCCCCAG CCCGGCTGAC CTCTGCTGGA GTTCAGAGAG GATGGGGGAC 240
GTTCCTGGCT GAGGGAAAGG CTCCTTGGAG ACGTCCCCAG GGGTCCGAGA CACGCAGGCG 300
TCGCCAGGGA CCGGGCTGTG TCCGGTGCCA GGGCTCAGCC AGGCCTGGAG CCAGGCGGGC 360
TCAAAGCCGT CTTTGTAGAG AGCTGTGGCC CAAGAAGCGT GGGCTCAGGG CCAGCAGAGG 420
GAGGCAGGGT CTGGGCACCC TGTGCAGCTG GGAGGGGTCA TGTGGGGTCA GATGGGGCCA 480
TTGAAGAGCA GCGTGGGGTT GTCTGTGCTC TGCTGTGGGA CCTCACTCAG CTCCCCTAAA 540
CCCTCCCAGC CTAAGACTCC TGCCCTGTAA AATCGGAATG GCCGTGTCTC CCATGAGGTT 600
AAGGGAAACC TCTGTTGCAC CTGGAGCACT TTGAGCCTGA AGCTACCTTG TAAGCTGGAG 660
GGAGGTTAGC AAGTATGGGA GAAGTGTTAG AGGCAGGACA GCCTCCCTCA GTCTTTCTTC 720
AAGGAGGAGA ATTTCCAAAG GAATTGCTTT CTCTTTTTTT TTTTTTTGTT TAGTACATAT 780
AGTTTGAAAC AGGGTCTCAC TCTGTCACCC AGGCTGGAGT GCAGTGGTAT GATCATCGCT 840
CACTGCAGCC TCGAACTCCT GGGTTCAGGT GATTCTCCCA CCTCAGCCTC CCATGTCAGG 900
GAGTAGCTGA GACCACAGGT GCGCACCATC ATGCCTGGCT AATCTTTTGT ACTTTTTTTT 960
TTTTTTTTTT GAGACGGAGT CTCGCTCTGT CGCCCAAGCT GGAGTGCAGT GGCGCGATCT 1020
CGGCTCACTG CAAGCTCCGC CTCCCGGGTT CACACCATTC TCCCACCTCA GCCTCCCGAG 1080
TAGCTGGGAC TACAGGCACC CGCCACCACG CCCGGCTAAT TTTGTTTTCG TATTGTTAGC 1140
AGAGACGGGG TTTCACCGTG TTAGCCAGGA TGGTCTCGAT CTCCTGACCT CGTGATCCGC 1200
CTGCCTCAGC CTCTCAAAGT GCTGGGATTA CAGGCGTGAG CCACCGCGCC CGGCCGGCTA 1260
TTTTTATATT TTTTATTTTT ATTTTTTCCT TTTTAGAGAG GGGGTCTCGC TATGTTGCCC 1320
AGACTGTTTT CTCTCCTTTA ATTTTTTTGC ATCCCCCAGT TAATTTCAAT ACCCACCCCC 1380
CCCCCCTTAC CCTAGCTCGG GGAGTGCCAC GGGAGAGACC TTGCCATGTT GCCTGTTAAC 1440
CTTGGCATAC AGTAAGCGCT AACAAGTGAT TACAAATATC AAAATAAACA CACACGGCGC 1500
CGCCCTCTGA GCCCGCCCCC GCTGACTTGC 1530