| Tag | Content |
|---|
EnhancerAtlas ID | HS132-00336 |
Organism | Homo sapiens |
Tissue/cell | Melanocyte |
Coordinate | chr12:133082550-133083910 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr12:133083699-133083713 | TATGCGGGGGCGGG | - | 6.17 | | EGR3 | MA0732.1 | chr12:133083699-133083714 | TATGCGGGGGCGGGT | - | 6.23 | | Klf12 | MA0742.1 | chr12:133083601-133083616 | GGAGAGGGCGTGGCC | - | 6.34 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_06575 | chr12:133081509-133085747 | Brain_Hippocampus_Middle | | SE_24669 | chr12:133082398-133082823 | Colon_Crypt_2 | | SE_24669 | chr12:133082856-133083153 | Colon_Crypt_2 | | SE_24669 | chr12:133083623-133083877 | Colon_Crypt_2 | | SE_32237 | chr12:133078546-133085188 | Gastric | | SE_41687 | chr12:133081655-133084777 | LNCaP | | SE_47660 | chr12:133082155-133084463 | Pancreas | | SE_65399 | chr12:133067333-133086073 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I132502 | chr12 | 133079421 | 133087879 |
|
Enhancer Sequence | TGCAGTGCTG GCTGGGGGTG TGTGGGCACA GGGGCTGCGC CTGGAGCCGG AGATGTCGGA 60
GGCCTCTCCT CCTCGGTGTG GGCACCCACC CCATGCTGTC TGTTCTCTAG AATGTTCACT 120
CAGCAGCACT TGTGAGCCCT GTCTGGGGCT GAGCAGGGGG CAGGACAGAT GGACATTCTG 180
GTGGGGGTCA GACGGGACAG GAAACTGCCT TGTGCTTGGT GTGACTGTGG CCGGGGTGGG 240
GAGGGAGCTG GAGGGTGGGT CTGTGGATGG GAGGAGGGGC CGGCAGAAAT CTTTATATTT 300
TTTTGAAAGC AGAGTAACAC TAGAGCAGGT TTACAGAAAA TGTGGTAAAT TTAAACAATT 360
TGCCCTTGAC ACATGCGTCC TTCTGGCCAG CTGTGAGCAC TGTGGCAATG GGGAGAGGTG 420
TGGAGCGGGC CTGGGGGAGC GTCTGTGCCC CGAGGGTACC ACCCGGTCCC GCCTCCTCAG 480
ATCTGCCCTC TGCCTGTCCC CTCTGACTCT TTGCCCAGTA GAAAGACAAA TCCCAGCACA 540
GTGGTGCCCT GCGTGGCAGG CTGCCCTTGC AGGTTTCCTA GTTACTGTGA AAGGTAACAC 600
CTTGATTTGT TCCTGCTTTT GATCCAGCGC TGCAAACAGC CGTTCTCTGG GCTGCAGCCT 660
TTGATTCATC CAGGCTGAGA CCCTCAGAGC TCACTGGGAA CCGTTTCTGC AGTGTTAGCA 720
GATTGCGTCC ACAGCTGCCT GGGATGGGCA GCCCTGACAG ATCCTGGGTG GGCGAGCAGG 780
AACTCTGGAG GCCATGGGCT CTCGGGCTTG TGCAGGAGCA GGCCGCTCAC AGCAGGGCTC 840
TGGGCCTTGA GTGGTGGCTC TGCAGAGAGC ATATGGCGGG AGCTGGGCCT CGGGGAGGCA 900
AGGAGTCTTC CTGGAGCCGG AAACAGCAAA GAGTTGGAGT GACAGGATCA GCCCTCGTGG 960
GCAGGGGGCC CGGAAACGCT GCTGGGCCTC TCAGGGCCTC CAGCTCAGAC TGGTGGGGGT 1020
GGCGCTTGTG TCATGGGGCG GGCGCCCAGC CGGAGAGGGC GTGGCCGGCA CCACCATGGC 1080
TCTTGTCTCT GTCGTCTGCC CTTACCGGAG GGACAGCCAA GGTCCTTCTC CCCAGGGACA 1140
CCATGGCTCT ATGCGGGGGC GGGTCCTCCT CGGGGACACT GTGGCCCTCC GTGGGGGCGG 1200
ATCCTCCCCA GTGGCTTCCC AGGGTTCTTG GCAGCAGCTC TGACATGGGT TCTGTCCTGG 1260
GCTTCACTGC TGCTGTTTTC CTCACAGCTG TGCCCTCCCC GAGAGGATTC TGTCCTTTCG 1320
TGGACGCTTC TCCCTGGCCG GCTGGCTCCT CTGGACCCTA 1360
|
