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

TagContent
EnhancerAtlas ID
HS050-71129 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr9:139759280-139760630 
Target genes
Number: 42             
NameEnsembl ID
SEC16AENSG00000148396
C9orf163ENSG00000196366
RP11ENSG00000227512
NOTCH1ENSG00000148400
EGFL7ENSG00000172889
MIR126ENSG00000199161
AGPAT2ENSG00000169692
AL590226.1ENSG00000221693
FAM69BENSG00000165716
SNORA43ENSG00000199437
SNORA17ENSG00000212487
SNHG7ENSG00000233016
LCN10ENSG00000187922
LCN6ENSG00000204003
LCN8ENSG00000204001
LCN15ENSG00000177984
ATP6V1G1P3ENSG00000224662
TMEM141ENSG00000244187
KIAA1984ENSG00000213213
C9orf86ENSG00000196642
NCLP1ENSG00000213212
C9orf172ENSG00000232434
PHPT1ENSG00000054148
MAMDC4ENSG00000177943
EDF1ENSG00000107223
TRAF2ENSG00000127191
FBXW5ENSG00000159069
C8GENSG00000176919
LCN12ENSG00000184925
C9orf141ENSG00000198454
PTGDSENSG00000107317
LCNL1ENSG00000214402
C9orf142ENSG00000148362
CLIC3ENSG00000169583
C9orf139ENSG00000180539
ABCA2ENSG00000107331
FUT7ENSG00000180549
NPDC1ENSG00000107281
MAN1B1ENSG00000177239
SNORD62ENSG00000199411
DPP7ENSG00000176978
GRIN1ENSG00000176884
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr9:139759295-139759310TGAACTCCTGACCTC-6.22
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9139760251139760347
Enhancer Sequence
TGGCCAGGCT GGTCTTGAAC TCCTGACCTC ATGATCCACC TGCCTTGGCC TCCCAGAGTG 60
CTGGGATTAC AGGCGTGAGC CACCGCGCCC GGCCAACATT TCTACCACTT CAGAGGAGTG 120
ACTTGTGGAG CATCCTAAGT GTGATCTGCT CACAGATGCT GCCACGCAAT TATTCCCATG 180
ACTCCTAGCT TGTGGCCATT AAGTTTCCTT TAAAAGAAAA GGAGAGTGAA TTTGGTTTTG 240
ACTGTGCAAC CAGTAAGGGT AGGGCAGACC AATGAATCCC TGTCACCAGA GCCCCAGCGC 300
ATCCTGGCCC AACTGGCCTC AAAGGCTTCA GCCCTAGGCC ACCTGAGGGT ACGAATGAGG 360
CAGAGGCGGT GACTAAACTG TCCTCCCTAT TACATCAGAC TCACAACTGA CCCTCGGATC 420
CATCAGCCAC ATTGGTAATC TCCTTCCACA AGTACTGTTC AGGGCACGCC CATCTTCCAC 480
CTGTGCAACA GGGTCCACCT GCTCATGGGG TCCCCTGAAG CAGGCACTCT CTACAGCCTG 540
TGATGCACCC AGGCAGGCTC CCTGGGCAGT ATCTGACCAG CGGAGACCAG TAGAACCAAG 600
CAGGTCCCAG GCAGAGAGAA AACTCTCAGG GAGGAGCCTA CCCCCTGTCC CCAGCTCCCA 660
CTCAGGTCAC TAACCTCTGC CCCGTCACCC AGTCTCCCGC CCCAGGCCCT CAACTGCTGT 720
CCAATGGCCC CCAGCCCTAT CCCAACCCCA ATTCCCCACC TTCATCGCTG GTTCCTGCTG 780
CTTGCCCCAG TCCCCACCCC TGTCCTAAGC CCTGTACCCC ACTCTACCCT GTTCTTCCAA 840
GCCCTGTCCC CATCTCCATC CCTGCCCCCG TTCCCAGTGC CCACCCTGGT TCTCTGTCCC 900
CTATCCTCAC ACAAGGCCCC CAGCCTTGTC CCCGTCCCCG TCCCCACCTC CTGCCTCTGT 960
CCTCACACCT GTCCCCACCA ACAGTCCCTG CCCCTATCCC CTCCCCGCCC CACCCTGGCA 1020
CTGGTCCCGG CCCTATCGCC TGCCCCTTGC CCCGTCCGGT TCCCTGCTCC TCTCCTCCTC 1080
CAGTCGCCCG CCCCCTGCCT CCTGGGTCCG TCCATCCCCT CCTGGGTCCG CCCCCCACCT 1140
TCCCACCCCT GTCCTGGCCC GGTCCTCCTA CCCCTGCGAT TCGCCCCGCC CTTCGAACCC 1200
CGTCCTGCCC CCGGCACCCC AGCCTTGTCC CCGTCCCCTG CGCCCTGTCC CAGGCCCCGC 1260
CTGCCCTTCC CCGAGCCCCC TGCCCCACGG TCCGTGGCCC CGGCCCAGCG TCCGCCCCGC 1320
CCGGCCCGGC CGCTCCTCAG TCAGCAAAGC 1350