Tag | Content |
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EnhancerAtlas ID | HS133-07088 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:13332320-13333020 |
Target genes | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr12:13332385-13332405 | CCCCACAACACACAAACACA | + | 6.22 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_00070 | chr12:13330671-13333635 | Adipose_Nuclei | SE_02366 | chr12:13331663-13333083 | Astrocytes | SE_26715 | chr12:13331506-13333248 | Esophagus | SE_36302 | chr12:13331995-13332979 | HMEC | SE_45692 | chr12:13331216-13333293 | Osteoblasts | SE_55863 | chr12:13331367-13333242 | u87 | SE_64909 | chr12:13331775-13332957 | NHEK |
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| 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 |
GH12I013177 | chr12 | 13330681 | 13333248 |
|
Enhancer Sequence | ATTTCTTTTT TTTTTTTTCC TTAAAGTGTT GCAAAACCTT AAAACTGTAA GGGAATAACA 60 GCTTTCCCCA CAACACACAA ACACAGCTCT CCTCTGGCAA ACAGGAAACA CTCCCAGGGC 120 TGTGGGCTCC TGAGCCAGGA AATGGGTCTT TGCTGCTCTG GTTACCTTCT CCTCAGGTTC 180 TTCCTGGGCA TTCAATGCAG TTAAAAATAG TAACCACCAA AACCAGAAGA AAAGATGATT 240 TCATTGTCTA ACCGCTGCAA CTTGTGGCCT GATTTGGGTG GTGGCAGAGA GGGAGCTAAT 300 CCTCTGAGTT GGCGCCTTGG GAATTCTCTT AGGGTCGAGC TGGTCCCTGC CCCAGGATTT 360 CAAAACGGGG TATCCCTGAG GAGCCAGCCC AGCTCAGGAG GGCGGCGTGT TAGGCAGAGC 420 CAGCTTACCA CACTCGTGCA CACTGTGGGT GAGGCAGCTG GTGGAAATGC AAGATCTCTC 480 CGTGGCCCAG CCTGTGAGCA GTGCAGGTGG CACACACCCG CCCTGGCTTG GGAAGGCAAG 540 GCTGGGGGCG GAGCCTGTCT GCTATCTGAG CTAGTCATTC CTGCAGTGGT CTGGGTAGTG 600 TGCATCCTCA GCTGGCCCTG GCAGGCATAA GAATTTGTAG AGTATGCTCA GTTCCACTCA 660 GCATAGGGAG CTGTCACAGT GACAGGTACA GAAGGGACCC 700
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