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

TagContent
EnhancerAtlas ID
HS105-40895 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr19:49458220-49458800 
Target genes
Number: 42             
NameEnsembl ID
EMP3ENSG00000142227
KDELR1ENSG00000105438
SPHK2ENSG00000063176
RPL18ENSG00000063177
FUT2ENSG00000176920
MAMSTRENSG00000176909
RASIP1ENSG00000105538
BCAT2ENSG00000105552
HSD17B14ENSG00000087076
PLEKHA4ENSG00000105559
PPP1R15AENSG00000087074
TULP2ENSG00000104804
NUCB1ENSG00000104805
DHDHENSG00000104808
BAXENSG00000087088
FTLENSG00000087086
GYS1ENSG00000104812
RUVBL2ENSG00000183207
LHBENSG00000104826
CGB2ENSG00000104818
CGB5ENSG00000189052
CGB1ENSG00000213030
CGB7ENSG00000196337
NTF4ENSG00000167744
AC008687.1ENSG00000225950
KCNA7ENSG00000104848
SNRNP70ENSG00000104852
LIN7BENSG00000104863
C19orf73ENSG00000221916
PPFIA3ENSG00000177380
TRPM4ENSG00000130529
AC011450.2ENSG00000235555
SLC6A16ENSG00000063127
CD37ENSG00000104894
TEAD2ENSG00000074219
DKKL1ENSG00000104901
CCDC155ENSG00000161609
PIH1D1ENSG00000104872
FLT3LGENSG00000090554
RPL13AENSG00000142541
FCGRTENSG00000104870
RCN3ENSG00000142552
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4645881chr1949458262hg19
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TP53MA0106.3chr19:49458470-49458488GGCAGGCCCGGGCTTGTC-6.05
Number of super-enhancer constituents: 2             
IDCoordinateTissue/cell
SE_28063chr19:49457050-49459256Fetal_Intestine
SE_39950chr19:49457283-49458876K562
Enhancer Sequence
TGAGGCGGGA GGCAGACGGG CGGGAGGAGG GCGAGCCCCC TCGCCGGCCC GTCCGGGATC 60
CTTCCTACCG GCCTGGGGCT GTGCGATCTC CAAGCACTGA GGGGCAGAAA CTCCCGGATC 120
GGGCGCTGCC AGCCTCCAGT CCCCTCCGTC CTCGGAGGTT CCTGGCTCTC TGATCCCCGT 180
GTCCCGATCC CTGCCTCTCT GGCGCTCTCG GACCCTCGAG AACCAGGGGA TCTCGGAAGC 240
CAAGCCCCCG GGCAGGCCCG GGCTTGTCGC CCGCACCACT TCCTGCCTCT GGCACTGGTG 300
GGAGGGGCGG GTCTCGCCTC TGCCCCCTCA GGCCAGGGGT CTGGATGCAT ATAGCGTTCC 360
CCTAGCCTCT TTCCCCGGGG AGAATGTAGG ATACAGGCCC AGCCTCCTGG CCTTTCTCCA 420
TCAGGGACTC AGTTGTCTGG GCCCCCCCGT CACTTTATCT GCTAGGGTCC CAGAAGTCCA 480
GGGTCCCCAG CTCTGTCCTC CCTCAGGGGC CGTGAGTCTC CACAGTCTCC TGATCCCCTA 540
GAACCCAAGA GTCCAGGTAC CTCTTCCCTT CCTTTCTCCT 580