| Tag | Content |
|---|
EnhancerAtlas ID | HS133-05384 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr11:18032670-18034490 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUND(var.2) | MA0492.1 | chr11:18032838-18032853 | TTAAATGAGGTCATA | + | 6.38 | | TFAP2C | MA0524.2 | chr11:18034225-18034237 | TGCCCCGAGGCA | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35602 | chr11:18032257-18034670 | HepG2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 18033400 | 18033779 | | chr11 | 18033800 | 18034338 |
|
Enhancer Sequence | GCACATGCAC ACATACACAC ACACACACAC ACACACACAC ACACCCCTAA CAAGGTAAAT 60
CCCCTTCCTG TGAACCGAAC TTTATTCCCC CAAAATTCAC GTGTTGAAGC CCTAACCTTT 120
AGTACCTTAC TGTATTTGGA AAGAAGGCCT TTAAAGGGGC AATTAAGGTT AAATGAGGTC 180
ATAAGGGTGG GGCCCTAATC CAATATGACT GGTGTCCTTA AAAGAAGAGA CACCACGGAT 240
GCTCACGCAC ACAGAAAAGG CCATGTGAGG ACACAGTGAA AAAAGCCATG TGAGGACACA 300
GTGAGAAGGC GGCCATCTGC AAGCCAGAGA GAGGCCTCGG GAGAAACCAA ACCTACTCAC 360
ACCTTGATCT TGGCCTTCTA GCCTCTGGAA CTGTGAGAAA ATAAATTTCT GTTGTTTAAG 420
CCTCTGTTGT GTGGTATTTT GTTATGGTAG CCCTAGCCGA CCAACACACC CCCACAGTTT 480
CAGATTATAC AGCAGGAAAA ACACACTACC AGTCCTCCAA ACACAGCAGA AGGGTGTCAA 540
CAACCTATTA AACATATTTT ACAACCTTTA ATATTCGGCT TTGTCTGTAC TGAAACAATA 600
TTTCTGTTTC CTCTGTCCAC ACAGACGCCA GTCTCCTGCC TGGAAAAAGC CAGAGACAGC 660
ACACATTCAA TCCCCAACTC CACCCCCAGC TCCCGGGCCA CCTCAAAGAC GCCCAGCCAG 720
CCAGACTACC GCAGGTCACG CCATGCTCTC CCTCCTGCCA AATTGCAGCC CCACATTCAA 780
CAATTGCCGC CTTGTACTGA TCATTACTTC TTTAAAAATT GGACAACTAA TACTGATTTT 840
AACAGCAATA CAGGTTATAA TTTTGCTCTC CCCCAACACA AGAGCTGGAA GTCCTTCACT 900
CGTGTATTTC ACTCATGTGT ATTTCCCCAA CACCAGCACA TGGGTAGGCA CACAGATGCT 960
CGTTCATTCA TTCGTCAACG AGTATTTACT GGGGACCTAC AATGTGCCAG ACACCAAGAG 1020
AGGCACCGTG AACAAGACAG GCACAGCACC CACTCTTACC ACACTTACTT TCCAGCCAGA 1080
GAGACTGACG TTAATAATAA ATTATACACA TCATTACAAT TGTGATACGT GCTATGAAGA 1140
AGCACAAGAC GCAGCGACTG CTTGTTCCCG TGCATGCTGG TCGGCCACCT GCCACGCTCC 1200
TGTGCATGAA CCCTCCTCTC TCCCAGACAC ACATCAAGAT GACCCTGTCT CTCCCAATGC 1260
TCCCGTCAAA CCAACAGCAG CCCAACTCCC CCAACACATG CAAGAACCGG TCACAGCAGA 1320
GTGTCAGCAA ATAGGCAGGG TCTGTGCCTT GTGCGCGGCC AAACACCGCA GGCCTCACAT 1380
CTAAAGGATG CTTTCGCCAG GCTGGGACAG GGTCTCCCTC CTCCAGGCAT CAGGAGTGTG 1440
GGGGGCACAG GTGGCCCCAC GGAGCTCTGG GACCGGGCGA TCCTCTCCAC CGAGCCCTCC 1500
GCGCTGTCTT CCAGGCGCTA TTCGGGCTGG AGGGCTCTCG CGGAACCAGA CGCTCTGCCC 1560
CGAGGCAGGT TCTTCCCGCG GCGCCACAGC CCCTCCGGCC CTGACCCCGC CAGCCGGCAG 1620
GCCCCTAAGT CGACCGCGAA GACCCTTCCT TCCCCGCCCG CCCGCTCCTC CTCCGCTCCC 1680
CCTCCGCTCC CAGCCCAGGA TCCTTCAACC CAGAGCCCGG CTCGGACCTC AGCCGCCCAG 1740
CCCCTGAACT GCCCACGCCG CGGCCAGCAG CTCCCACATC TCGGCGCCCC TCAGGGCCTG 1800
CACCGGCCCG GGGGCGGAGT 1820
|
