| Tag | Content |
|---|
EnhancerAtlas ID | HS133-16408 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:12465090-12467300 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr2:12466389-12466402 | GAAGGTTCTAGAA | - | 7.12 | | TCF3 | MA0522.2 | chr2:12466609-12466619 | AACACCTGCT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_56492 | chr2:12465113-12467040 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I012325 | chr2 | 12465927 | 12466597 |
|
Enhancer Sequence | TCAGCCTCCA GAGTATCTGG GATTACAGGC ATGCACCACC ACACCTGGCT AAGTTTTGTA 60
TTTTTGGTAG AAATGGGGTT TCACCATGTT GGCCAGGGTG GTCTCAAACT CCTGACGTCA 120
GGTGATCCAC CCACCTCGGC CTCCCAAAGT GCTGTGATTA CAGACATGAG CAACCGTGCC 180
TGGTCCCAGC TGGTAGTCTT TAATAGCTCT TCTGGTGATT CCAACATGCC ATCAGGGTTG 240
AGGGCTATTG ACCCAGGACC AGGGCTTTCA GAGCCAAGAA ACAGGATTCT GCCTCACATA 300
CCAGGCTCTT TCCACCCTGC CTCAGTCAGA GGAGCCACTT TCTTCACTGG TTCCTCAGTC 360
TCTTTTGCTC AGGTACTGGT TCTCCTTGGC TGCTCTTCTG CTGATTTTGG GGGGAGCTTA 420
AACAATACTA ATGCCCAGGT TCCAATGCAA GAGATTTTGG TTTGCTTGGT AGGAGGTAAT 480
CAAAATTGCA AATGCAGAGT ACAGCCTGGG CATCAAGGAT TTCTTCCCCA GGAAATTCTA 540
AACAACCATT CAAGGAGTCC CACGTATTTA TTCAAGCCTT CAACTTACAT TAGGTTCATG 600
AGAAACTTAC CTTCTAAGCT GCAGTTTATT TGTAAATCTT GCCTCATTAG GGAATATGGT 660
ATTGCCAACA TACTTGTATT TCCTTGATAG GGAAAAAATG TGTACCACAA AGTCTTCCTT 720
AATAAAGTGA ACCACTTAGA CCCTCATGCT TGGATATTTA TTCCTGCCAG AAACGTGTAT 780
TGACCAGCTT CCATCCCATG CCATGTGAGC AACCCATGCA GTCCCACAGG AGAGAAAAGG 840
GTGAGAAGAC ATTGTGTCTC TGCTTAAGAA AGTTACTGTC GAATAGAGAA AGCAGATAGT 900
AATGTCACCG TTATACAAAC ATGGTGATTG CTGGAGGCAG GCGGTGGAGA ACAAGAGCTG 960
TATGAGCCCA GAGTATTTCT CAAGGTAGAA AAAGGAGTCG GGAAAGACAT GCGGGCAGAC 1020
ACGAGAGCTG CACTAAGGCC CAGCTGTGTG ACGGTTGGTG AGGCGCTCAG GAAATGCCAG 1080
CCTCTGGTGC TGGTGAGTCA CTGAGTTCAT GGGAGGAGTG GCTGGAAAGC TGGTTTGAGA 1140
TTAGATAGTA GAGAGCCTCG TAAGCTAGAC TAAGGAGTTG GAAGTTTTTA AAATAAGCTC 1200
TAAGGTTTTT ATGAGAGATA GAATTTACCA ATGTTTTAAC AAAAATTATA TGAAAGCAAG 1260
CAAAGGGCAG CATTGGGAAG AGGGAGGGCA GACTCAAAGG AAGGTTCTAG AAACATCCAG 1320
GGAAACAATT ACAAAGACCT GAACTAGGGA ATTGACAATG GAAATTAACA GAATGGAAAA 1380
GATGGAAAGC AGGAAATAGA CGAGCCTAGG TAAGTGGCAG AGCCAGCACT TGAATCAGGG 1440
TCTTGGCTCT CATTTAACAT GCACCCAAAC AGAAACATGC AGACACACAC ACAGACACAC 1500
ACACACACAT AGACACATGA ACACCTGCTC ACACACACAC ACACGCATAC ACGCATGCAG 1560
AGACACAGAC ACACACAGAT ACACATGCAT ACAGGCACAC ACAGAGACAC AGACACAGGC 1620
ACTTGCACAG ACACACACGC ACACACACAC ACCGAGGGCA GAATATGTGC CACTCACTGG 1680
CCAGATCCTG GGGACATAGA GATAGATATG GTTGCTGGCC TCATGGTGCT TACAGTTGAG 1740
AGGGGGAAAT TGATAGATAG AAAGCCAGAG AACGTTACTG AAATAAGCAA AGGAGAAAGA 1800
CAGGTGGACC AGACTTACAG GGGATAAAGC TTTTGGGATA AAGCTTCTCG AATGAAAAAA 1860
ACATCTAAGA GGGTATCAGA AAAGTCAGTG GGAGTGAAAG GCTAGAAGGG CAGACAGGGG 1920
AGGGAGGTTG GGCTCCAGGC AGAGGGAATG GCAGGTGGGA AGCCCAGAAG TGACATTGCG 1980
AGAGCACACA TGAGTGCGTC TAACTCCACT GAATGAGCTT GGTATGGCAC CACCAAGCGG 2040
TAGCAAAGAT GGTGGTGGGA AAGGAACCTG GAGAGGTGAG CAGGGCAAAT TTGACAGTGC 2100
CTATCTCCGT CCTGGAACTG ACTCTCTGCG GAGCTCTGAA CAATGGCAAA GGCGTGCACC 2160
CCTCTTCTCC CCAGCAGGCT GCTCACAGCT ATGCCTAGAA TAGAGCACAT 2210
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