| Tag | Content |
|---|
EnhancerAtlas ID | HS133-24592 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr5:657050-658690 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr5:658147-658157 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr5:658147-658157 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr5:658147-658157 | ATTTTCCATT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_04867 | chr5:657066-658754 | Brain_Cingulate_Gyrus | | SE_05836 | chr5:657189-658980 | Brain_Hippocampus_Middle |
|
| | 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 |
| GH05I000656 | chr5 | 656799 | 658746 |
|
Enhancer Sequence | ATCAATAATT CGCCTCAAGA ATGGATGACT TTTATCACTT TTTCTGCAGT GATGGAGATG 60
ACCATGATTT TTATCATTTA ATATATTGAT GTGTTTAACG ACCATAATTT GCTTTTGTTA 120
AAAATAAACC TTGAATTTCT GAGATAAGTC CAACTTAATA ATTATGGATT TTCTTTTACA 180
TACATATTGT TATATTTGGT TTGTTAATAT TTTGTTTAGC ATTTTGTGGC CCAGCTATAC 240
TACCTAGCAC CTGTGTTTGG GCCCTGATTT CCTCGTCTGT ACAATGGGGA AATAGTGGCT 300
TCCTCACAGG ATTGTTGTGA AGGTGAAATG AGTTAGTATG AATAAGACTC TCGGGCAGCA 360
TCTGGTGCGT CCTGAGCACT GGGTAGCTGC GTGCTCTAGT ACAGTGGTTA GTATCTCTCT 420
TCACGGGTGA CAGCCACTTA CGATTTTCCT TTGTAATGCT GTTCTTGAAA GGATTCGCAT 480
CTTTACACCA CCGTAAAATG AGCTAGGTTG TGTATTCTTT CTCCATTCTC TAGGAGAATT 540
TACTTAAGAT TATAATTATT TCTTCCATGG ATGTTTGATG GAACTTGCTG GTGAAGTCAC 600
TTGTGCCTGG AACTTTCTTT GTCAGGAGGT TTGACTACTG ATCCAGTATA ACTCAGTGTT 660
CCAGGATGTG GCAGAACCGT TCACACAGAC CATCCTTATG TCCCCCCTGC CTTTACGCTG 720
CATATCCCTG AGTTGGGCTG GGGCCGTGTG ACTACTGAGC AACAGCCTGT GTGTGGGACT 780
GAGGTGAGTC ATTTCAGGGC CAGAGCAGCG GGAGCTGGTG CGTCACTGTG ATAGCTTCCC 840
TGCCAGTGAC CTGGGCAGCT GCATCACAGG ATTAGGAAGT CTGTTTGTCT TCTGTTAGAA 900
GAGATCTCTT GTTATTCCTG AAGTTGGACG TTGTGTGAGT AATACATTTT GTGTGTCCAG 960
CCACTGAAGT GTTAGGGGTT TTCTTTTGTA GCTGGCAGTG ACTTCCCCTA AGTCACAGGG 1020
CTGAGCAGGC TTTCCATTTC TTTTCGAGTT AGTTTTTGTA AGTTATGTGT CTCTAAGAAT 1080
TGGTCCATAT TGTCTTAATT TTCCATTTTG GGGGGTATAA CACACATAAT TTGAATGGCT 1140
TCAACATTTG AAGTTGTGTG TGTCCCTGTG GCAGAGATGT AGGGACAGTT GTGTCCCTTC 1200
AAGCGAGACC TTGCCATCCA GGGGCAGGGA GTACAGGGGT AGAGACCATC TCCAGCCACC 1260
ATGCTGTCAG GCTGTGCCTG GGCTCTGGAG CTGAGGACAC ACTCATCCAG GCAGCTGCAG 1320
CCAGTGTCCA AGCAGGCAGG GCCTGGGCCT AATGCGAACC ACAGGGAGCT CCCTAGCAGG 1380
TCATCTCCAG AGCCTCCCTG AGGCCTCCCG GCCTCCTCCC CTTGCTGCTG TTCAGGGGCA 1440
TTCCTCACCA GTGAGCCTCT TGTGATACAA AGGCCACCTC AGCATCTGCC TCCCGGGGAC 1500
TCAGCCCATT CTTGGCCATT CTTCATATTC GTTATTTGAA CTTTCTCTTC AGTCCTTTCA 1560
AAGAAACACC CTTTGCCTCC ATTTTCTTTT CAATTTCTGA TCTGATCTAT CATTAGCCAT 1620
GCTGAAATTA CAAATAAATA 1640
|
