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

TagContent
EnhancerAtlas ID
HS121-38135 
Organism
Homo sapiens 
Tissue/cell
LNCaP 
Coordinate
chr9:140006680-140007190 
Target genes
Number: 51             
NameEnsembl ID
EGFL7ENSG00000172889
AGPAT2ENSG00000169692
AL590226.1ENSG00000221693
FAM69BENSG00000165716
SNORA43ENSG00000199437
SNORA17ENSG00000212487
SNHG7ENSG00000233016
LCN15ENSG00000177984
ATP6V1G1P3ENSG00000224662
TMEM141ENSG00000244187
KIAA1984ENSG00000213213
C9orf86ENSG00000196642
RP11ENSG00000228544
NCLP1ENSG00000213212
C9orf172ENSG00000232434
PHPT1ENSG00000054148
MAMDC4ENSG00000177943
EDF1ENSG00000107223
TRAF2ENSG00000127191
FBXW5ENSG00000159069
C8GENSG00000176919
LCN12ENSG00000184925
LCNL1ENSG00000214402
C9orf142ENSG00000148362
C9orf139ENSG00000180539
ABCA2ENSG00000107331
FUT7ENSG00000180549
NPDC1ENSG00000107281
ENTPD2ENSG00000054179
SAPCD2ENSG00000186193
UAP1L1ENSG00000197355
MAN1B1ENSG00000177239
DPP7ENSG00000176978
GRIN1ENSG00000176884
LRRC26ENSG00000184709
TMEM210ENSG00000185863
ANAPC2ENSG00000176248
SSNA1ENSG00000176101
TPRNENSG00000176058
TMEM203ENSG00000187713
NDOR1ENSG00000188566
RNF208ENSG00000212864
C9orf169ENSG00000197191
RNF224ENSG00000233198
SLC34A3ENSG00000198569
TUBB4BENSG00000188229
FAM166AENSG00000188163
C9orf173ENSG00000197768
NOXA1ENSG00000188747
WDR85ENSG00000148399
ZMYND19ENSG00000165724
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
STAT3MA0144.2chr9:140007042-140007053TTTCTGGGAAG+6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9140006869140006922
Enhancer Sequence
CCCTGGGGAG GAGAGGCGCT GGGGCCCAGC GGCCACACAC AGACACACCG CGGGCTCCGG 60
CCACCAACCT GTCCCCCCTC GGAATGGTCC TGCAGGGGAT CTGGGGCTCT GGGATCTGTA 120
GGTCCCAGTG AGGAAGGCCC TCCAGGCTAC CTGCTTGGAG GTCGGCGGTG TCTGTGCTGC 180
CAGCCCCGGG CCTGACTGTT GAGGGCCCCC CCGCTCTCCA CGGGGCAGGG TGGGGCCTGC 240
TGCCCTCTGT TGCCCTCCAT GCTGGGGACC CCAGGGGCCC CTTGGGCAGC ACCCACCAAG 300
CTGGGCCTGG CTACAGCCAG TGCTGAGAGG GTCCCCAGGG ACGGCCCCTG CCTCCCCCAG 360
GGTTTCTGGG AAGGTCGTGC TGTCCACCCC ACCACAGCCC TGGGGCAGGA GGCAAAGCCC 420
CTGGCCGGGC TGCGGATCCT CGCCCCACCC GGCCCCAGGA CCCAAGCCAA GCCTGGGGTC 480
TCCACACTTG CCCATCTGGG GCCGGGGGAA 510