| Tag | Content |
|---|
EnhancerAtlas ID | HS133-07750 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:68758400-68759580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr12:68759158-68759173 | GACCACGCCCTTTCC | + | 6.75 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_09841 | chr12:68750615-68762761 | CD14 | | SE_13065 | chr12:68756652-68759676 | CD34_Primary_RO01480 | | SE_13536 | chr12:68755624-68762644 | CD34_Primary_RO01536 | | SE_14207 | chr12:68756789-68762675 | CD34_Primary_RO01549 | | SE_39838 | chr12:68755890-68760485 | Jurkat | | SE_44133 | chr12:68757089-68760390 | MM1S | | SE_49866 | chr12:68754291-68762684 | RPMI-8402 | | SE_55049 | chr12:68757981-68760044 | Stomach_Smooth_Muscle | | SE_66689 | chr12:68755890-68760485 | Jurkat |
|
| | 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 |
| GH12I068361 | chr12 | 68755615 | 68762621 |
|
Enhancer Sequence | TAATTGAATG CTTTACAATG GAAATATTTT ATAAATACAA AAAGAAAAAC ATCTGAAGAA 60
ACTCAATATC AGCGCCATTT CTACTGAAAA TTTTTCATCT TGCAGTTTTA ACTTCTCACA 120
GAATCCTTTC CTTTGGACTT GAGGCCTCTG AACCTGTGCT AATTGCACTC TGTCAGGAAT 180
TCGTCCTTGG CGACCATAGA AAATATTACA GGTGTCTGTG CTACCCAGAA AGCAAAGGGT 240
TGTGGTGCTT TCTTTTTTCC TTTGAGTTAC ATTGCGACTG GCACAGTTAT GAAATGAGAA 300
ATGTTACACA CAAGATTGCC ACAATCCCCA TTTTTGGCTT ATCTTTATGT CCCATACATT 360
CTTTTAAGAT TTCTATCGCC TCAGTATTGT CGATTTCCAC ATCCACAGCC TAACAACGTG 420
GTGCAATCGC CCTTTGCGAC GCCGCAGACC AACAGACGGA TGCTGCCCTG CTGCAGTTTC 480
ACAGCACACC GGGTCTTTCC GCTTCAGCTG GACAGAGGCC CAGCCAGGCC GTAGGGAGGA 540
TTCCGAAGGT CTCTCTGCAG AGGACCGGCC TCTCAGACCG AGAAGGCTCC ACCCAGGCAG 600
GAAAGGACAC TGTATGTGGG GCAGTCGGCC TGGGCCCCAT GGCTCGTGTT TGTTGCTGAA 660
TTGGGCAACG TGGGCTGCGG TTCACAGGGC AACAGAGACT TCACCACCTA ACACATCGGG 720
GCTGGTGCAG CTGAGGAGGG CTGCTTCTGC CTCTTGGTGA CCACGCCCTT TCCCAGGCTG 780
GGCCCACAGG AAGTCTGGCC GGGAAGGGAG GAGGCACTGC AAGCTGTGGG AACCACACCG 840
GCTCCTTCAC TGCTGACAAA GATCTACTCC ACCCCCACCG AGAAACTAGC TCAGAACCAG 900
CTTTCCTCCT CCTCCGCAGC CCTCATGCCC TGAATGGCTG ACTTGGGGGA TGTTTACACT 960
CATTTTTTTC ATACTTAAGG GGGTGTGGGT GCCAGATCAA CTTGCTCACC ACTCAGACCG 1020
CACACAAGAA GCCTTATGTT GAAACTTGTT CAACCTCCAG TAACCAAGTC ATGCAAGTGG 1080
AGAAAACTAG ATAGCATTGC ACACACACAT ATACATACAC AGGCATATAT AGACACATAT 1140
ATATCCATAT ATATGTGTTT ATGTGTGTGT GCAATTATCT 1180
|
