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

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EnhancerAtlas ID
HS133-17032 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr2:65258640-65260030 
Target genes
Number: 11             
NameEnsembl ID
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RUNX1MA0002.2chr2:65258724-65258735GTTTGTGGTTT+6.02
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr26525977565259992
Number: 1             
IDChromosomeStartEnd
GH02I065030chr26525780165260188
Enhancer Sequence
CCCATGCCCA CCTTCCCAGC TGCAGCTTCT GAGTTTCACA CAGGTGCTCT GCTTGGCAGA 60
CCTGCAAGGA AGTCTGAAAA AGCAGTTTGT GGTTTTCCGT CTGTGCAGCT CAGGAAGGTA 120
CACCTGATGG GAGTTAGCTG GGCTTTGGCT AGCCAACCTG CAGGGTCTGG AACTGCTTCT 180
GTTTGCAGGA CGCATCCCCC TATTCCAGAC AAGCTCTGGA TTCCCCTAAG TGCCTATTAC 240
ATGACAAAGG CAGGCTTTGT GAATGAGCGA ATACATCAAA CCCTCTCATA GTGCTGCTGC 300
CTACCAGCCA GTGGGTCTGT TTCTGTGCTG CCACCAACTT TGTTGAGCAA TATTTGTCTT 360
ACAGCTATTT TGAGTATTTT ATTGCACTGC CTTTGTTCTT TTATTCCACC CCTCTTCCTC 420
TCTCTCTAAG TGAAAGAAGT GAAGTAACGA TATTTGTGAT AAGAAGTGTA GTCTCATACA 480
TTTTATGAAA CTGAAACAAT TAAAATTACC AGTAGTATCC GAAGCAGCCT ATCTATATCC 540
TCAATGAGAC CTCAGTGGGA AAAAAGATCT ACTGCCTCTT CACCTGTAAA TAACACGTGA 600
AACTGCTAAG ACCGTGTTAT TGAAGAATGT GGCTAGTGGG CAGAGTGCCA TTTGGAATTT 660
TATAGTCGTC ATTATCTTTC TGGGAGTGGA ACCTCCCTTA TAACGTGGAA GGCTATTTTC 720
AACTTTTGCA CTTTTTTACT TGGATGCCTT TTCCAGACTC TGTTAACGTT TGGAATTGGG 780
TTTCACTCTA CAGAGAAAGA GAAGCAGGAG GACAGGTGTA GAGGGGAGGA GAGGGAGGAC 840
CGTGGGTCGC AGATTGGGCC TATTCCCCTG CACTCACCAC TTTGTCTGTC ACTGCCAGCC 900
CGCTCCCCCC TTTTCAGATA CCAACACCAG GCCAGGGGTG ACAGCCCAGG AAGGTGGCAT 960
CCACAGCCCT CAGCCCTCTG TCCTTGTCAT TCACTCCTAC CAGTCCTCAG CCCTCTTATC 1020
TGTCTGGGAG TGAGATGAAG GGCAGCTGGA AGCGGGAGGA AAGGTCCTCT CCTCTCCACT 1080
ACAGTGACAA GAGGTTTGGA GGAGCTTCTG GGTGAGGCTT AGGGGGTGAC CCTCCTGTGC 1140
AGAGCGGCAT GGGCTACAAA AGAGTGGATG TTTGTCCTGT GTGTGGGTCC CTCCTGGGGG 1200
CTAAAATGAA ATCTCCTTTC ATTTTCTGAT ATCATGTGAT CTCTGACTTA CAAACCTACT 1260
TTCCTGTGCC ATTTCTGTCT AAGACAACAG TCGCTTCTAA CAGAGCCAGA GTCCTACATT 1320
ACTGAGGAAA CCACCACCAT ATCCCATGCA TGAAAGGGCC GGCCTGTTGT GAATAACAAA 1380
CTAGTGGCCT 1390