| Tag | Content |
|---|
EnhancerAtlas ID | HS133-05661 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:57333400-57335050 |
Target genes | | Number: 18 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:57334782-57334803 | AAAGCGAAATTGAAACCAGTT | - | 6.2 | | IRF1 | MA0050.2 | chr11:57333784-57333805 | GAACAGAAAATGAAAGTAGAA | - | 8.18 | | ZNF263 | MA0528.1 | chr11:57334995-57335016 | GGAGGAGGGAATGCGGGAGGC | + | 6.13 | | ZNF410 | MA0752.1 | chr11:57334615-57334632 | TCAAATTATGGGATGGG | - | 6.29 | | ZNF740 | MA0753.2 | chr11:57334417-57334430 | CCGCCCCCCCCCC | + | 6.64 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCCCCAACAT ATAATATAAA CACATCCCAT GCCCCCCTCC TATCCCTCAG CCTATGTTCT 60
ATTTCTGTTC AACCAATAAG CTGCTTCTGG TGCCTTCCAC CCAGGGTCAA TGGCCCTTCA 120
TTTATCTTTA CCCCAAACTA GAAGCATCTG CACTTGTAAG AGTTTCTCTA TCATCTGTGA 180
CTCTTTGGCA AGAACAAAGC CCAGGGCTGA CCGGAGAAGA TCTGGAATAG ACATTTTCCA 240
GGTCTTGGAA AGATAAAGAC ACTTGAACTT TATCTGTTTA GGATGAGTTC TGCCAGAACT 300
TTCCCAAAGC CTGAGGAAGT TGAAACCCAA CCTAAAACAC ACAGTTCTTT CCTACTGCCT 360
ACTAGGAAAT CACCTGACTC AGAGGAACAG AAAATGAAAG TAGAAAGGCC ATTAAGAGAG 420
CCTGCAGGCT GGAGGCCTGT GGACCTGGTT TCATATTCCA GTCCCATTGC TCCTTACTGA 480
AAGACTCTGG ACAAGCAAGT TATTTCCTCT GTGCCTCAAT TTCCTCATTT GTAAAATGCG 540
GGTATATATT ACTTATCTCA CAGAACTGCT GTGCGAATTA GATGAAATAA CCATGTAAAC 600
CGTTTGGCAT GTAATGGTTC CAATGCAATA AATTCTGGCT CCCATCTCTC TTCCACTTGG 660
CTGGAAAGAC CCTCTGCCTC ATTTTGCTGC CAACCTCCAG ATTTAGTATC TAGGCCAAGC 720
CTGCTCTGGG CATCCCAGTC TGAGGCCATT TTCTTCTCAG AGGCTGAGGG TAGCAGGCAC 780
CCTCTTCCTA GAGCCTGCCC CTCCACCCTG CAGACTGGAA GGGGCACTTC TGAAAGACTT 840
GGGGTGCCAG ACTCACTTCA CCAGGATCAC CTTCCTCCCT AATCCATCTC CAAACACCCT 900
GGGTTTTCCC ACCTTCTGGA GGAAACTGCC CCCTCCCCAT CCTTCCAGAT CTTATTTCAA 960
ATTGTGTCCC TGATAGGAAC AAAATTCAAC AAGGGCCGGA TTTGTGTTCA TCTCTGCCCG 1020
CCCCCCCCCC CCTCCTAGAA CAGGGCCAGC ACATGTAGGC ATTCAACACT TGTAGAACTC 1080
ACGAACGCAA GCCACCTACT CCAGGAGGCC TTCCAGGTCC ACCTCCGCAT CTTTTCCTCC 1140
AGAGAATACT CAGGGAACTT TGTCCCAAAT TCTAATCAGC ATTCCGTGTT TCTCAGGACT 1200
CTAGTAATAC AGGCATCAAA TTATGGGATG GGCTATGGGC TTATTCCAAG GCAAGGACTT 1260
CATCCTGGTC ATCTGTGTTC ATAACCCACC ACCAGCAGTA GCAGAATGCC TGGCACCAAG 1320
ATGCCAAGGA CTTTTCCTGC ACTGGAGATG CACCCAGTTG TTATCACAAG TTTCAGGCAG 1380
GAAAAGCGAA ATTGAAACCA GTTTTGGGGG AGCCGGCTCA TCTTCACCAC GCGAACGGCT 1440
CAAGCAGAGG CCTCCAAACC CCCAAAACCC CAGCTCTGGC CACTCTTGCA GGCCAGTCCT 1500
CCTCTGAGTA GAGGGCGGGG AGGACAGGGA TTCAGCCAGC CCTGGTGCCC AGACAAATAA 1560
ATAAATGTGC TCGGAGAGCC GCGGAGGGGA TGGAGGGAGG AGGGAATGCG GGAGGCGAGG 1620
GGAGCCAAGA GAAAGGGGTC ATCCTATACG 1650
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