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

TagContent
EnhancerAtlas ID
HS133-31382 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr8:144902880-144903760 
Target genes
Number: 42             
NameEnsembl ID
ZFP41ENSG00000181638
GLI4ENSG00000250571
RP13ENSG00000253716
ZNF696ENSG00000185730
TOP1MTENSG00000184428
ZC3H3ENSG00000014164
7SKENSG00000221399
RP11ENSG00000254144
GSDMDENSG00000104518
C8orf73ENSG00000204839
NAPRT1ENSG00000147813
TIGD5ENSG00000179886
EEF1DENSG00000104529
PYCRLENSG00000104524
TSTA3ENSG00000104522
ZNF623ENSG00000183309
ZNF707ENSG00000181135
FAM83HENSG00000180921
SCRIBENSG00000180900
PUF60ENSG00000179950
NRBP2ENSG00000185189
EPPK1ENSG00000227184
PLECENSG00000178209
GRINAENSG00000178719
PARP10ENSG00000178685
OPLAHENSG00000178814
EXOSC4ENSG00000178896
CTDENSG00000255224
GPAA1ENSG00000197858
CYC1ENSG00000179091
MAF1ENSG00000179632
SHARPINENSG00000179526
FAM203AENSG00000235173
TSSK5P1ENSG00000227473
HEATR7AENSG00000179832
AC145291.1ENSG00000204775
FAM203BENSG00000230567
BOP1ENSG00000170727
HSF1ENSG00000185122
GS1ENSG00000254690
DGAT1ENSG00000185000
TONSLENSG00000160949
TF binding sites/motifs
Number: 17             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr8:144903121-144903139GGGAGGGAGGGAGGAGGG+6.27
EWSR1-FLI1MA0149.1chr8:144903097-144903115GGCAGAAAGGAAGGGAGG+6.69
EWSR1-FLI1MA0149.1chr8:144903109-144903127GGGAGGGAGGAAGGGAGG+6.88
EWSR1-FLI1MA0149.1chr8:144903113-144903131GGGAGGAAGGGAGGGAGG+6.92
EWSR1-FLI1MA0149.1chr8:144903101-144903119GAAAGGAAGGGAGGGAGG+7.08
EWSR1-FLI1MA0149.1chr8:144903117-144903135GGAAGGGAGGGAGGGAGG+7.08
EWSR1-FLI1MA0149.1chr8:144903105-144903123GGAAGGGAGGGAGGAAGG+8.62
SCRT1MA0743.1chr8:144903572-144903587GAGCAACAGGTGGGA+7.46
SCRT2MA0744.1chr8:144903572-144903585GAGCAACAGGTGG+7.22
ZNF263MA0528.1chr8:144903095-144903116GGGGCAGAAAGGAAGGGAGGG+6.06
ZNF263MA0528.1chr8:144903693-144903714GGAGGAAGAGCGTGAAGAGGA+6.59
ZNF263MA0528.1chr8:144903115-144903136GAGGAAGGGAGGGAGGGAGGA+6.63
ZNF263MA0528.1chr8:144903107-144903128AAGGGAGGGAGGAAGGGAGGG+6.64
ZNF263MA0528.1chr8:144903102-144903123AAAGGAAGGGAGGGAGGAAGG+6.72
ZNF263MA0528.1chr8:144903690-144903711GGAGGAGGAAGAGCGTGAAGA+7.72
ZNF263MA0528.1chr8:144903114-144903135GGAGGAAGGGAGGGAGGGAGG+7.9
ZNF263MA0528.1chr8:144903111-144903132GAGGGAGGAAGGGAGGGAGGG+8.23
Number of super-enhancer constituents: 6             
IDCoordinateTissue/cell
SE_03846chr8:144902624-144903251Brain_Angular_Gyrus
SE_03846chr8:144903359-144906283Brain_Angular_Gyrus
SE_05376chr8:144900910-144913651Brain_Cingulate_Gyrus
SE_06345chr8:144900347-144913365Brain_Hippocampus_Middle
SE_07205chr8:144900997-144912535Brain_Hippocampus_Middle_150
SE_25185chr8:144902135-144907808Colon_Crypt_3
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr8144902909144903208
Number: 1             
IDChromosomeStartEnd
GH08I143820chr8144902747144908263
Enhancer Sequence
TGCCATCTGA AAGACAGTAA AGACAGAGTT CAGTCTGTTG GAGCCGAGCA GTCTCCCGCT 60
CTCGTCAACA CCTCACGCAG ACAGCGGCAA GGCCCGGAGT CCCCGCCCTG CCAGGGAGGC 120
CGCCTGCCTT CCCACACTGC CGGCCGCCAG CACCTGCCCA GGGGGGCCGC AGCGCCCCAT 180
GTGCCCCGCC CTGCAGCCTT GCAGCTGGGC CGGCTGGGGC AGAAAGGAAG GGAGGGAGGA 240
AGGGAGGGAG GGAGGAGGGC AGTGGAGCAC AGTGAATGGC CAGGACATCT CCTGGTAGCG 300
TGAATGTCTG AGGGCTGGGC GGGGGGGCGT GAGGCTCGAG GCCCAGGAAC CTGTCGGCCT 360
CACACCGGCC TCTTCCCACG AAGGTATCGC AGCCTCCGGC CACAGGCCTG GAGCAGGGCC 420
CCAAGGGAGG TGCCTCCAGA CTGTCCCCTC AGTCCTGGGG CTGAGCCCAG GTGGTCTGGA 480
CTCACTGCAG GGGTGAGGGC CTGAGCAGTC TTATCCAGGC CACGGGGGCA GGGAGGCCCA 540
CGCCCTGCAT GCTGCCACCA TCGGCTGTGC ACAGCTGGGG CAGGGAGCAC GGGAGAGACC 600
AGAGGCCACA GTGTGAAGAC CAGGAAGGGG AAAAGGGTAG AGCTGCAGCC AAGCAGCCAA 660
GAAAGGGGCT GCGGCGCTTT AGGGGCTCCA GCGAGCAACA GGTGGGAAAG GCTGGGCCAC 720
TCGTGCCTCA GAGAGGACCC CGGGGGTCCC GAGCATGAGT CTTTGAGAAT CGGAGCACTG 780
TAACAGCTTG CGGGGACGGC CGCAGGCCCA GGAGGAGGAA GAGCGTGAAG AGGAGGAGAT 840
GGTGGCTGTG GTGGGGAGGG CGGTAGAGGC TCCGGCCGGG 880