EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-00702 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr1:25056470-25057900 
Target genes
TF binding sites/motifs
Number: 18             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NR2C2MA0504.1chr1:25057716-25057731TGAGGTCAAAGGGCA+6.86
Nr2f6MA0677.1chr1:25057717-25057731GAGGTCAAAGGGCA+6.65
RxraMA0512.2chr1:25057717-25057731GAGGTCAAAGGGCA+6.62
ZNF263MA0528.1chr1:25056836-25056857GGAGGGGGAGGGGAGGGGGAG+6.01
ZNF263MA0528.1chr1:25056847-25056868GGAGGGGGAGGGGAGGGGGAG+6.01
ZNF263MA0528.1chr1:25056823-25056844GGAGGGGGGAGGGGGAGGGGG+6.03
ZNF263MA0528.1chr1:25056824-25056845GAGGGGGGAGGGGGAGGGGGA+6.08
ZNF263MA0528.1chr1:25056810-25056831GGAGGGGGAGGGGGGAGGGGG+6.37
ZNF263MA0528.1chr1:25056830-25056851GGAGGGGGAGGGGGAGGGGAG+6.65
ZNF263MA0528.1chr1:25056844-25056865AGGGGAGGGGGAGGGGAGGGG+7.23
ZNF263MA0528.1chr1:25056839-25056860GGGGGAGGGGAGGGGGAGGGG+7.49
ZNF263MA0528.1chr1:25056850-25056871GGGGGAGGGGAGGGGGAGGGG+7.49
ZNF263MA0528.1chr1:25056807-25056828AGGGGAGGGGGAGGGGGGAGG+7.67
ZNF263MA0528.1chr1:25056813-25056834GGGGGAGGGGGGAGGGGGGAG+7.97
ZNF263MA0528.1chr1:25056833-25056854GGGGGAGGGGGAGGGGAGGGG+8.18
ZNF263MA0528.1chr1:25056820-25056841GGGGGAGGGGGGAGGGGGAGG+8.19
ZNF263MA0528.1chr1:25056802-25056823GGAGGAGGGGAGGGGGAGGGG+8.37
ZNF263MA0528.1chr1:25056827-25056848GGGGGAGGGGGAGGGGGAGGG+9.41
Number of super-enhancer constituents: 7             
IDCoordinateTissue/cell
SE_03668chr1:25056864-25057733Brain_Angular_Gyrus
SE_04517chr1:25056867-25058172Brain_Anterior_Caudate
SE_05379chr1:25056417-25058249Brain_Cingulate_Gyrus
SE_06312chr1:25055251-25058327Brain_Hippocampus_Middle
SE_07165chr1:25055397-25058025Brain_Hippocampus_Middle_150
SE_08484chr1:25056421-25058225Brain_Inferior_Temporal_Lobe
SE_41323chr1:25056830-25057633Left_Ventricle
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr12505688025057476
chr12505661725056885
Number: 1             
IDChromosomeStartEnd
GH01I024730chr12505687925057792
Enhancer Sequence
ATGGTGGCTC ACGACTGTAA TCCCAGCACT CTGGGAGACC AAAGTGGGCG GATCACCTGA 60
GGTCAGGAGT TTGAGGCCAG CCTGGCCAAC ACAGTGAAAC CCTGTCTCTA CTAAAAATAC 120
AAAAATTAGC AGGGCATGGT GGCGGGTGCC TGTAATCCCA GTTACTTGGG AGGCTGAGGC 180
AGGAGAATCA CTTGAACTGA GGAGGCTGAA GCAGGAGATT GGCTTGAACC TGGTGGCAGG 240
GGGGTGGACG TTGCAGTGAG CTGAGATAGC GCCATTGCAC TCCAGCCTGG GCGACAAGAG 300
CCAAACTCCA TGGTGGGGGG AGGTGGGGAA GCGGAGGAGG GGAGGGGGAG GGGGGAGGGG 360
GGAGGGGGAG GGGGAGGGGA GGGGGAGGGG AGGGGGAGGG GACTCCTTCT CAAGCCTCAC 420
CTAAAAATGA AGAGGCAAAC AAGGTGGGAA AAAAATAAGT GTCGAGCTCA ACCCTTAGGA 480
CCCTGGCCAT GTCTGCAGTC AGCTCAGGCA AGGCTGTTGT CCTTCTGTAA TGGACTGTCC 540
CTGGTGCGCT CTCAGACGCA GCAGGACACG ATGCGGCAGG ACCCAGTGTT CCACGCAAGG 600
ACCTGCAGTC CTGGTTCAAA TCCAGACACT GCCATAGGAA GCTTAGCTCT ACGTGAGGAG 660
ATTAGCGACT GTTCCATGCG GGAAACAAAC CAACCAAGCC AAAGCCTGCA AGTCTCTCCC 720
AAGCTGCCAG CAAGTGAGCC AGGTGGACCT CCAGGGCGTA GGATGCAGCT GGGAAAACAA 780
CCGACCCGCT GCTTTTCCGG GTCCCTGCGC TTGCTGCGTC TCCTCTGGCT GCAGAGACTC 840
AGCCCGGCTC AGAGCTGGGG AACTCGGTTA TTCTTTTGAA GCGTCAAGGG CACTTGTCAG 900
CTTTGAAATA ATACATTTGC TGGCTTGAAT TTCAAATAGC TTAACGCCCC CTGTGCTACC 960
TAGCTGTGAT CTGAAGGACT GACTGTTCAG GCCTTCAAGT ACCAAATAAA TGAACCATGA 1020
GACTCCAGCA ATGGAGAAGA AATGTCCTTA TTCAAACCAA ACTTTGCAAA TGGAAAGAAT 1080
TGTTAAGTTT TGCTCTGTTG TGGCAGGGAA GCAGCTGGGA AGTAGACCAC CCCTTGCATG 1140
CTCTGGGGGC CAGAGCTGGC TGTACTTGCA CCTTTAGGCA GTAGGAAATG CACCCCAGCT 1200
CTGTGGTGTG AGCCACTTCT CCGTGATGAA GGTCATCTTC ATATTCTGAG GTCAAAGGGC 1260
AAATGGCAGA GTGGGCATCC GTGGGGAGAC TGCTGGACAC AGGGCACTGC CCACAGAGAG 1320
GTGATGGGTG ATAGGAGTGG GGCAGGACAG CATAGCAAGG TGCAGCATCT GGAGTCAGAA 1380
CAGACAGGTT CAAATCCCAG CTCTGCTGCT TACCTACTAA GCTGTTTGAT 1430