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

TagContent
EnhancerAtlas ID
HS133-16857 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr2:46774220-46775110 
Target genes
Number: 10             
NameEnsembl ID
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
HNF4GMA0484.1chr2:46774518-46774533TGACCTTTGGCCTTC-6.43
NR2F1MA0017.2chr2:46774550-46774563CACTTGACCTCTG-6.62
Nr2f6MA0677.1chr2:46774518-46774532TGACCTTTGGCCTT-6.73
RxraMA0512.2chr2:46774518-46774532TGACCTTTGGCCTT-6.09
Number of super-enhancer constituents: 14             
IDCoordinateTissue/cell
SE_09677chr2:46770088-46777270CD14
SE_10431chr2:46773990-46777378CD19_Primary
SE_11068chr2:46767730-46780807CD20
SE_20419chr2:46774035-46777126CD56
SE_30489chr2:46773668-46777340Fetal_Muscle
SE_40865chr2:46773678-46784358Left_Ventricle
SE_42711chr2:46773796-46780337Lung
SE_48469chr2:46773700-46777382Psoas_Muscle
SE_49217chr2:46773895-46777190Right_Atrium
SE_51656chr2:46770078-46780437Skeletal_Muscle
SE_54157chr2:46773825-46777410Spleen
SE_58655chr2:46761142-46803039Ly1
SE_60213chr2:46761079-46802912Ly4
SE_62608chr2:46761090-46803268Tonsil
Number: 1             
IDChromosomeStartEnd
GH02I046546chr24677374046777329
Enhancer Sequence
TTTGACAGAC AAGTAGGGTA TGTAGGCTTC AGTTGGTTCT ACTTTCAGAG AGTTAAGATG 60
GAATGAGGCA GCTCATGGCA CTACAGGTCA GTTGCCTTCT CTCCAAAATG TTCACTCATG 120
CATGTGGGCA CTCATTGTAT TTGAATAACA GCAACAGTGC CTCCCTCAGT TTGGAACCTC 180
TAGTCCACTT GCTCACTCAT GGTCCCTGCC TTAACCCCAG TCAAGTTCAA AGCCATAGGC 240
ATCATTTGTC CGACTGACAT ATTAGGGCAT CTACCAGTCA AAGGGTGATT GTTGTAGATG 300
ACCTTTGGCC TTCTAGAGCA GGCTGCTTTC CACTTGACCT CTGCTGCTAT TAGCAGACAA 360
AGAGAGAGAA TGGGAGAGAG AGTGTATTGG ACTTCAGTCC CCATCATGTG CACTGCCTGG 420
GGACATCCCA GCACACTCAG AGCACCACTG CCAAAGGGAA CACTTCCCCT CTGTTGGCCA 480
AGCCCATGGG TGGTCCAGGA GCAGCTGTCA CATTTTGACT GCCAAGCATT TTGGAGTGGA 540
AGTTGACCGA GGCATCTTCC TTCTCACTAG GGGCCTTGCG TGTGTTTTGG GGGTGAGGGG 600
TTGGCTTCCT GCCTGGGCCT CTGTGGAGCT TCTCCTTTCT TGCCCAGCCT TCAGGACTTC 660
AGTGTAGGCT CTGCAGCAAC CCCATTGTCT GCTCAAGGAG GGACTGGAGA GATGGGATTT 720
TCCCTCCTGC TACTGCACTG TTTGGAGCGA TGGGAAGTGG AAAGAGCTCT CCCTCTCTGT 780
CCAGACAGGC CAGTGGGGAG CTGCCTGGCA AGCTGCTCTC TAGCTGTGGG CTCTAGGCTG 840
ATCTCTTAAT CCTTGGCAGG AAGGCAGAAC TTGATACCCT GGAGAGGGAA 890