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

TagContent
EnhancerAtlas ID
HS108-41942 
Organism
Homo sapiens 
Tissue/cell
K562 
Coordinate
chr9:140323840-140325230 
Target genes
Number: 44             
NameEnsembl ID
ATP6V1G1P3ENSG00000224662
TMEM141ENSG00000244187
C9orf86ENSG00000196642
PHPT1ENSG00000054148
FBXW5ENSG00000159069
PTGDSENSG00000107317
C9orf142ENSG00000148362
ABCA2ENSG00000107331
RP11ENSG00000231864
SAPCD2ENSG00000186193
UAP1L1ENSG00000197355
MAN1B1ENSG00000177239
DPP7ENSG00000176978
snoU13ENSG00000238824
GRIN1ENSG00000176884
LRRC26ENSG00000184709
TMEM210ENSG00000185863
ANAPC2ENSG00000176248
SSNA1ENSG00000176101
TPRNENSG00000176058
TMEM203ENSG00000187713
NDOR1ENSG00000188566
RNF208ENSG00000212864
C9orf169ENSG00000197191
RNF224ENSG00000233198
SLC34A3ENSG00000198569
TUBB4BENSG00000188229
FAM166AENSG00000188163
C9orf173ENSG00000197768
COBRA1ENSG00000188986
C9orf167ENSG00000198113
RP13ENSG00000260996
NRARPENSG00000198435
EXD3ENSG00000187609
NOXA1ENSG00000188747
ENTPD8ENSG00000188833
NELFENSG00000165802
MRPL41ENSG00000182154
WDR85ENSG00000148399
ZMYND19ENSG00000165724
ARRDC1ENSG00000197070
C9orf37ENSG00000203993
EHMT1ENSG00000181090
SETP5ENSG00000233998
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF14MA0740.1chr9:140324846-140324860GGCCACGCCCCCTC+7.52
KLF16MA0741.1chr9:140324847-140324858GCCACGCCCCC+6.62
SP1MA0079.4chr9:140324844-140324859CTGGCCACGCCCCCT+7.26
SP3MA0746.2chr9:140324846-140324859GGCCACGCCCCCT+6.82
SP4MA0685.1chr9:140324826-140324843CTGGCCACGCCCCATTG+6.17
SP4MA0685.1chr9:140324844-140324861CTGGCCACGCCCCCTCG+7.46
SP8MA0747.1chr9:140324847-140324859GCCACGCCCCCT+6.92
Number of super-enhancer constituents: 1             
IDCoordinateTissue/cell
SE_23952chr9:140324302-140324815Colon_Crypt_2
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr9140324299140324790
chr9140324856140324948
chr9140324031140324195
chr9140324315140325145
Number: 1             
IDChromosomeStartEnd
GH09I137429chr9140324303140324815
Enhancer Sequence
GGTGGGGACG GCGTCCTGGG GCATGGCGGC TGGTGCTGAG CCCTCGAACT GTGTTCCCAG 60
GGATGGGGGG AGGTGCAGTC CAGGCCACCG TAAGGGCCAG GAGGGTAGAG AGTGGGCCCA 120
CAGCCATCCT CAAACTGGCG CCCACGGTAG GGGGGCGGTG CCCCAAATGG GGCTGTGAGC 180
TTGAAGGCAG AGCCCACTAG AGCCGGCTGC ATAGGAGGGG GCTCCAGCTC TCTCAACAAG 240
GACCCTGCAG GTGCCACCCC GCCCCCAGAC TGGGCCATGG CCACAGCCAC AGCCTTGCAG 300
CCTCCCAGAG TCCCTGCGTC TCTCTGCGTC CTTTCATGCC TTTGTGTCTC CCTGTGTCCC 360
TGCCACAGAC AGCGAGGTCC CGGGGGGGTC CCTGCGTCCC TGCCACAGAT AGCGAGGTCC 420
CGGGGGGGTC CCTGCGTCCC TGCCACAGAT AGCGAGGTCC CGGGGGGGGG GGGTCCCTGC 480
GTCCCTGCCA CAGATAGCGA GGTCCTGGGG GGATGCCTGT GTGCCTGCCA CAGATAGCGA 540
GGTCCCCGGG GGGGTGCCTG TGTCCCTGCC ACAGACAGCG AGGTCCCAGG GGGGTGCCTG 600
TGTCCCTGCC ACAGGTAGCG AGGTCCCGGG GGGGGTGCCT GTGTCTCTGC CACAGCTAGC 660
GAGGTCCCGG GGGGCGGGGG TGCCTGTGTC CCTGCCACAG ATAGCGAGGT CCCGGGGGGT 720
CTCCCTGTGT CCCTGCCACA GATAGCGAGG TCCCTGGGGG GGTCCCTGTG TCCCTGCCAC 780
AGATAGCAAG GTCTCACGGG GGCAGGGGCT GCAGTCCGAC GGTCTGGGCC ACGTCACGCC 840
CACACTTGGG TCAGAGCCAG GCAACACCCC TAAAGTCACA GGAATGGGGA GCTGCTCACC 900
CCCAAAGGCA GCGGGCGAAA CATGGCGGAG AAGAAGAACT CCTGGTGGGC AAAGACTGGG 960
TCACCCTTGG CTGGCCACGC CCCGGACTGG CCACGCCCCA TTGGCTGGCC ACGCCCCCTC 1020
GGTCACCTGC GCTGCGCCAC GGCCGACTCC TGGGCCCAGT GCAGCTGCCC AGCAGGGGAG 1080
GCCTGGGGTG GGCGAAGCCG GGCTCTGAGC TGTGTTAATG CATTAACTTA GAGTCCGCAT 1140
ATCACAGTAG AGTGCTGTTT ATAAGAAACC AAAATGTTTT TAAAGTTGTG CTAAAAATAA 1200
GTTAACATTG CAGCAGATGT TTTTCTCCAT CAGACATTTC CCTCCATGGT GGTCTGGCAG 1260
ACGTGGGCCG GGCATGGGCA GCTGTCACCC AGCCCCCGGG GACTTAGAGC TGCGGGGCAC 1320
GGTGGGGCGG GCTGCAGGGA GCAGACCCTG CTGGGCCGCT GATCCCTGAC CCAGCGTCCC 1380
CACTGTCCCC 1390