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

TagContent
EnhancerAtlas ID
HS050-71111 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr9:139569260-139571030 
Target genes
Number: 40             
NameEnsembl ID
GPSM1ENSG00000160360
INPP5EENSG00000148384
SEC16AENSG00000148396
RP11ENSG00000227512
NOTCH1ENSG00000148400
EGFL7ENSG00000172889
MIR126ENSG00000199161
AGPAT2ENSG00000169692
AL590226.1ENSG00000221693
FAM69BENSG00000165716
SNORA43ENSG00000199437
SNORA17ENSG00000212487
SNHG7ENSG00000233016
LCN10ENSG00000187922
LCN6ENSG00000204003
LCN15ENSG00000177984
ATP6V1G1P3ENSG00000224662
TMEM141ENSG00000244187
C9orf86ENSG00000196642
NCLP1ENSG00000213212
C9orf172ENSG00000232434
PHPT1ENSG00000054148
MAMDC4ENSG00000177943
EDF1ENSG00000107223
TRAF2ENSG00000127191
FBXW5ENSG00000159069
C8GENSG00000176919
LCN12ENSG00000184925
C9orf141ENSG00000198454
PTGDSENSG00000107317
LCNL1ENSG00000214402
C9orf142ENSG00000148362
CLIC3ENSG00000169583
C9orf139ENSG00000180539
ABCA2ENSG00000107331
FUT7ENSG00000180549
NPDC1ENSG00000107281
ENTPD2ENSG00000054179
SAPCD2ENSG00000186193
MAN1B1ENSG00000177239
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr9:139570096-139570116CCCCCAGCCACCCCATCACA+6.43
Number of super-enhancer constituents: 9             
IDCoordinateTissue/cell
SE_23641chr9:139569149-139571142Colon_Crypt_1
SE_23982chr9:139569426-139569874Colon_Crypt_2
SE_23982chr9:139569988-139571173Colon_Crypt_2
SE_28198chr9:139568342-139571915Fetal_Intestine
SE_29345chr9:139568530-139571723Fetal_Intestine_Large
SE_40809chr9:139547596-139569983Left_Ventricle
SE_42234chr9:139547415-139572027Lung
SE_47596chr9:139569922-139570820Pancreas
SE_53640chr9:139549025-139570450Spleen
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr9139569967139570727
chr9139570136139570301
Number: 1             
IDChromosomeStartEnd
GH09I136673chr9139568079139571827
Enhancer Sequence
TGCAGGCAGG GAGACGCACA GCTGAGGCAG CCCTGGGGAC AGGCCAGGCA CACCCCAGGC 60
TGCATGTGGT TGGGGAGCCC TGTCCTGCGG CCCACCCACC CCTGCCTTCG CTGCTGCCAT 120
GGGTCCTTGT GGCTGTCCTG CCCCTGGGAC CTGGGATATG TGTCCTGCTC TGGTTGGCCC 180
AGAGTTCCAT AAGCTCATCC TGCAAATTTT TACTCATCTC CTCTAGGAAG CCCTCCTGAG 240
CTAGCACGTG TTTGCCTGGT TCACACCTGT CCCCATATTG GGTCTGCAGC TAGCCAGGGG 300
GGCAGGGCCC TGTCCGGTTT AGGAGGAGAT TATGGCACTC TTCCCTGCCC ACGCCTCTCT 360
CCCAGTCCTC TCCATCTCAG GAAGCCAGTG AGGGAGGCAG CCCTAGCCCG GGGGAGGGGT 420
GGAGCCTGCT GGTGTTCCTG GAAGTCACCG GGGTCAAATC CAAGGGCACT TGGGGGTGAT 480
CATTAACCCG AGGCAGCCAG GGAACCTCCA GGGGGCCAGC AGGTAGGCTG GGGACTGGCA 540
GCAGGAAGGG AGGGGGCCAG CAGGTAGGCT GGGGACTGGG AGCAGGGAGG GAGGGGGCCA 600
GCAGGTAGGC TGGGGACTGG CAGCAGGAAG GGAGGAGGCC AGCAGGTAGG CTGGGGACTG 660
GCAGCAGGGA GGGAGGAGGC CAGCAGGTAG GCTGGGGACT GGGAGCAGGG AGGGAGGGGG 720
CCAGCAGGTA GGCTGGGGAC TGGCAGCAGG GAGGGAGGGG GCCAGCAGGT AGGCTGGGGA 780
CCGGGAGCAG GGACGGAAAA GCTGTGGGTC TCCTGGCTGA AGCTGCACTG CGGCCACCCC 840
CAGCCACCCC ATCACAGCCG CCCGTCTCCC CTCTGCTCTC CCAGAGCTGA TCCAGCCCTC 900
ACTCTGCCCC CAAAGGGAAG TGACATCAGC CCCAGGCTGG GCAGGTGTGC CCCGCACCTG 960
GGCAGGGCTG GGATCAGAGC CCAAGGATGC TCACCCAGCC CAGCGCCTCC GGGGCTCCCC 1020
AGGCCTCACG GCCTTAGCTG GGAGCCTCTG GAAGGAGGGC CCCCTCCCCA CCACCTTGCA 1080
CAGGGCCAGG CACTGGGGGC CACTAGTGGC CAGTGTGAGG GAAGGAGCTG AGACCCCTGC 1140
CCTGAGCGAG ACCCCACCCA GATGGGTAAA AGCTCCTTCT CCTGACGCAA CTCTTCCCAG 1200
CACAGCGGCA GAGGCAGGAC AGGTGCTGGG GGAATGGCTA TACCCTGGCC TCTCCCAGAC 1260
ACCCTAGGAT GCACTGCACC CCTGGAGGCT GGGGACCAGG AAGTCCAGAG TCTGGAGGCG 1320
CTGCTTACAA TGAGCTCCAC CCACCCTGAG CTCTGGTCTG GCCTGATACT ACACCAAAAG 1380
CCTGGCTTGT CCAGACCCAC TGCCCATGCC CTGAAGCCCA CCCCAGCCAG GCACAGGCCC 1440
AGAAATGAGC CTCCTGAGAG CTCTGCAGCA GAGGCGAGCG GCCCGGCTCC CCACCCCTCT 1500
ACCTGCCCAG CCTCGCAGGC CAAGCACTGG GTGCCCACCA AGGGCAGCTG GTCACTCTGG 1560
GCTCTGTGTG GGCAAAAGGC CCAAGGGGCT GCCCTCCCTG GTCGGTCAGG GGGCAAGTGC 1620
AGGAAGGGGC AAGGAGGCCC TGTCCCCAAC TCAGTGGGAG GAGTCCCTTG TGTGTCAAGG 1680
GTCCTCAGCT CGGCTGGTGG TCACCTGCTG CCTTAAGCCA GCCTGACCCC GCCTCCCCAG 1740
CCTGCACCCA CCCAGGGAGG GCTGGGCTCA 1770