Tag | Content |
---|
EnhancerAtlas ID | HS133-32258 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr9:127596570-127597950 |
Target genes | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr9:127596756-127596768 | AAACAAACAAAC | - | 6.32 | Hnf4a | MA0114.3 | chr9:127597650-127597666 | GCCAGACTTTGACCTC | - | 6.01 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_29813 | chr9:127596526-127598359 | Fetal_Muscle | SE_37410 | chr9:127596212-127598086 | HSMMtube | SE_48044 | chr9:127597188-127597636 | Pancreas |
|
| Number: 1 | ID | Chromosome | Start | End |
GH09I124834 | chr9 | 127596356 | 127598614 |
|
Enhancer Sequence | GAGACCCCAT CTCTACAAAA AAAATTTAAA AAGTAGCCAG GCATGGTGAT GTGCATTTGT 60 GGTCCCAGCT ACTCAGGAGG CTGAGGCGAG AGAATCACCC GAGCCAGGAG GTCGAGGCCG 120 CAGTGAGCCA TGATTGCGCC AGGCACTGCA GCCTGGGCAC CAGAGTGAGA CTCTGTCTCA 180 AAAACAAAAC AAACAAACTA AACTCAATTT CCAGATGGAG GGGGAGCAGT AGCTTTGAGG 240 AGCTGTGAGA GCCTTTGTAA GTGGCATTTG ATGGGCACAG CGACAGGGAA CCAGGCAGGG 300 ACTAGACAGC AGCTTGTTCT GCTGCAGAGG CTGGAACCGG GCAGCAGGGA GCCACAGGAG 360 AGGACCAGGC TGGGAGCGTG TTACTTGTGG GGCTGGGGCA CTGGGCTGGG AAGGGGCAGA 420 CTGCCGAGGC TGAGGGTGGG GCAGGGTGTG AGAGCCTGGA ATCTGAGCTG GGTGGGATGG 480 GGGCAGGGTT CCAATCCAGC CATGAGCTCA GGCGAGTCCC TGCCCCTCTG AGCCACACTT 540 TCATCTGTCA AATGGGGCCA ATGACACATC CGATGACTCA AAGAACACTT GCACTAATAA 600 GGCTGTTAAG AGAATCTGGA GGCCCGGCCA GGTGTAGGGG AGAAGCTACT TACGGAGCCA 660 CCTGACTGCA CCTGAGACAG AGTCCCAGGC AGTGCCAGAG GGCAGGGGAC CTCCTGAGCC 720 TGGCATCTTG GCCTTCCCTC CTGAGCTCCC TCCGACGCAG AGCAGACCCA AGCAGCTTCC 780 CCGGGGCCCT AAGTGGGAAG CACGTTTTCC AGCCTAGGGA TGGACACGGC CCTGGTGCCA 840 GTGGCACTGT AGAGGGGCCC CTGTAGGTGA GGCTGCCCTC CCAGGCCCCT TCTGTACGCC 900 ACCCTGGTGC CGTGCTGACC ACTCGCTGAG ACACACCATA AACCCTTCCT CCGCCAACTG 960 GTTTCAGAAT CATCCCACGT TCCTCACCAG GCCCCAGGCT CCAGGTCTGG GTGTACGGGG 1020 AGTTTTCCCT GTAGCCTGGC TCCCCGCCAG CCACAGAAGC CTGTTGGAGG CTGGCACACA 1080 GCCAGACTTT GACCTCTGGG GAATTTGTTC TAGAGTTTTA TTAATAGCAA CAATATCTTG 1140 CATTTACTGT GTGCCGGGCT GAACTACACT CTACTTGCAT AGAAAATGCA CAAGGACCCT 1200 GTGAGCTGGG GTCCATGATC CCACTCCTAG GAGAGCAGAT GTCAAGTTCC CCACCCAGCC 1260 TCACACAGTG GGGATCCCGC TTGGGCAGCC TGGCACCAGA TGACCCTTTC TCAGGGACTG 1320 CACTGCCTTT GATTTTGTGG GAAGAACACT GGTTTGAGAG TCTGTAGCCC TGGGTTCTGC 1380
|