| Tag | Content |
|---|
EnhancerAtlas ID | HS133-18329 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:238511440-238512940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr2:238512822-238512833 | AGCCTGAGGCG | - | 6.14 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_29379 | chr2:238508569-238513274 | Fetal_Intestine_Large | | SE_29932 | chr2:238511899-238513200 | Fetal_Muscle | | SE_36919 | chr2:238511882-238513478 | HSMMtube | | SE_38427 | chr2:238511360-238514349 | HUVEC | | SE_42111 | chr2:238511874-238513499 | Lung | | SE_51094 | chr2:238511649-238513003 | Skeletal_Muscle | | SE_63809 | chr2:238512087-238512831 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 238512238 | 238512938 | | chr2 | 238512118 | 238512869 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I237599 | chr2 | 238508356 | 238513672 |
|
Enhancer Sequence | TGTCCTTTGT AACATCCTTT ACAATAAGCC AGCAAACATA GTTATTTCCC TGAGTTCAGT 60
GAGCTGCTCC AGCAAATTGA TCAACACAGA GAGGAGGTCA TGGGAACCCC AACTTGAAGC 120
CCATCCGTCA GAAGTTCGAG AGGCCCAGGC TTATGACTGG TGTCTGGGGT GGGTGGCAGT 180
CGTGGGGACT GAGCCCCCCA CCCAGTGGGA TCTGGTGCTA TCTCCAGGTG GACAGTGTTA 240
GAATTGAACA CCCAGCTGGG GCCCACTGCT TAATGTGTGG GGAAACCCCC ACGCCTTTTA 300
TTGCAGACGT CTTCTGTGTT GATGATTGTG GAGGTGGTGG TGGAGTGAAA GAGGAAAAAC 360
GCAGTTTGAG AGAGTTTTTC CATACACACC AACAAACCAG GGAGGTGGAT ATTGTTATCC 420
CCATTTTACG GATGAGAAAA TTGAGGCTCA GAGAGATTAA GTACATTCCC CAGAGTTACG 480
TAGCTATCGA ACAAGGATTC AAATCCACAA CTTTCTTAAC CTACCCCACA GAGGCAAATG 540
CAAAAACCAA ACCATAAGAG GGAGGAAATA ATGACCTCTG CAAATGAAAG CCACCTGTAT 600
ATCAAGAAAA GCATATGGAT AAAACAAAAT GCTGGGACAA TAACTGCCAC AAACATGTGG 660
CTTTAAAATC CTTGATTTAT AAATCAGCAA AAAATGGACA AAGGCACAGC CAGACAATTC 720
GCTGAAAGTG AGTCCCAGGT GTGCAGGCAG CGCTAGCAGG AGCGTTCGGC CTCACCAGCA 780
CGTGCAGGAG CCGGTCAGCA TGGAGGTCAG ATTGGCAAAG CCTCATCACA TCCAAGCTTT 840
GGCAAAACAG TAGAGACTGT CCACCAACCG TTGCTGAGAC TGTCTGGCAG TGCAGTTTTC 900
TGAGAGGGCA AACCTGGGAT GCGTAGCAAT GAATTCAACA ACACAGCCTT TGACTCGGCA 960
ACTGCACGTC AAGAAACGGA ACTGTCAGGA AGCATCTAGA ACCCAGAGGG CAGAATCCAG 1020
GAAATGACTC TGTTCCGGAG TTCATCTGTT GCTCTGGGCT ACACTTGATG CTACGGTAAA 1080
ATCACTCACC CTCACATCCA GCCAGCGGCA ACACACACAA TGAAAACCGT TCTGAAAAAG 1140
CAAAGCTGAG AGCCCCGGGA AGATGCAGGA GGTGTGGGTG GGGGTTGGAA TTCAGCTCGG 1200
TTTAGATAAA CAACTGAGAC CCGAGATGTT GATCTCTAAG GATTATCTCA GCCCCGACCT 1260
ATTTCAACTT CCTTGTCTTC TTTCTTTGGC TCCTTACTTT TCATTGAAAT TCCCTGACTG 1320
GCCCACTAAG AACCAGGCTC TGGCCAGCAC GGTGGCTCAC TCTGTAAGCC CAGCACTTTG 1380
GGAGCCTGAG GCGAGAGGAT GGCTTGAGGC CAGGGGCTCG AGACCAGCCT GGGCAACATA 1440
GTGAGATCCC CCCAATCAAT TTTTTTTTTT TTTTAAAAAC ACCCTTTTTT TTTTTTAATT 1500
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