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

TagContent
EnhancerAtlas ID
HS121-38130 
Organism
Homo sapiens 
Tissue/cell
LNCaP 
Coordinate
chr9:140003640-140004990 
Target genes
Number: 50             
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
WDR85ENSG00000148399
ZMYND19ENSG00000165724
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr9:140004079-140004093GACCACGCCCCCTC+6.89
KLF16MA0741.1chr9:140004080-140004091ACCACGCCCCC+6.14
KLF16MA0741.1chr9:140004636-140004647GGGGGCGTGGT-6.14
SP3MA0746.2chr9:140004635-140004648TGGGGGCGTGGTC-6.16
SP3MA0746.2chr9:140004079-140004092GACCACGCCCCCT+6.29
SP8MA0747.1chr9:140004080-140004092ACCACGCCCCCT+6.52
Znf423MA0116.1chr9:140004675-140004690TGCCCCTTGGGGGCC-6.01
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9140003726140003886
chr9140003864140004148
chr9140004301140004360
chr9140004756140004885
Enhancer Sequence
ATGTCGCCTG TGTCTTTAGG GATCTCCATG ACTGGAAAGT CTGGGCGGAC GTTGGGGAGA 60
AGGTATTCTT CAAGTCACGT CTCAGAATTC GGTTTGCTGA GACTGGACTC TAGCTGTCCC 120
CTGCTGGTGG GCAGGGAGAG GCCACGGGGA AGCTCCGTGT CCCTGGCCCC ACGGGGCAGA 180
TGCTTGGCGG GAGGCATCCT TGCGCCTGCG TTTCACACAG GGCCTGTTTC CCTGCAGGGC 240
TGGCACTGAG GCGCACAGCT GAGGGATACA CGGGCCCTCA GGTCAGGCAG CTCCCAGCAG 300
CCTGGCATGG CTATGGCCCC GAGCCCTGGG CTGTGGTGGC AGAGTTGTCC TCATCATCAC 360
TCTACTGCTG TCCCTATCCC AGGGCTGACC CTGGGCCTTG GCTGGGTTCC CCCCGACCCT 420
GAACCAGGTG ACCTCTTAGG ACCACGCCCC CTCGCTCTCC CCTGTGAAAA ATCCATCACC 480
TTCACTTCCG GAAGACTCCC CTTCCCTGGG AAGCCAGAGC CGGTGGCGGC ACAGGGCAGG 540
GCTACCCGGA CCCAGCCCAG GATTGCCAGC TCCGCCCCTC GGGACGTCCG GGCCCCGAGT 600
GTGGGCCTCG GCTCTGCCTG TCCCCACAAC CCCCAACATC CCACAGCAGC CACCTGTGTC 660
CCTCTGGGGA CAGTGGGCAC CCTGGGGCTT CGTCTCCCAC TTCATGCTGG GCCCTGATCC 720
TGCACTCCAC CCTCTGTGCC TGGAAAGGTG AGAACATCGG CTGTCATGTG ACCCTGGCGC 780
CTGCCCCTTG TCACGGTGGG CCCAGCACGG CCCTAGCCTG CCCCTTGTCA GTACCACCCT 840
AGCCCGCCCC TTGTCACGGT GGGCCCAGTG CTGCCCTCCT GGACCAGGTG CCCCATGGCC 900
GGCTGAACGG GCAGGACTAG GGCAGCAGGT GGGGCCTCAA CAGCCGGAAA AGGTGCACCT 960
TCTCCATCTC ACCCAGACCT CCGAGACTAA CGTGCTGGGG GCGTGGTCCC AGAGGGTGGA 1020
GGGACAGCAA CTGCATGCCC CTTGGGGGCC AAAAGCACTG TCCAGTGGCC TCCCCTGGAG 1080
GGGTCGCTGT GTACAGAGGA TGTCAGGGAA GGAGTCACCT TGGAGGTGTG GCTGCAGCCT 1140
CTGTCTGCTG CGGCTCAGCA GAGCGGGGCT TCCTTGCGGG GCACTGCCCC CCGCTGCCCT 1200
AAGGAGCAGA CCTGAGCGTT GTGGAGCCTC TACCTTGTGG AGCACATGGC ATACCCGGCC 1260
TGTGTGGGGT GCGCCGCGTC CCCAGCCGTG TCTCCGAGGG TCCCGCTCCC ACAGCCTGCG 1320
TGTGGGCCCC ACAGACAGGA AGGACGGGAC 1350