Tag | Content |
---|
EnhancerAtlas ID | HS133-25799 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr5:157037950-157040150 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr5:157038641-157038652 | CTGCAGCTGTT | - | 6.02 | Tcf12 | MA0521.1 | chr5:157038641-157038652 | CTGCAGCTGTT | - | 6.62 |
|
| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_52470 | chr5:157038548-157041466 | Small_Intestine | SE_59459 | chr5:157019018-157041234 | Ly3 | SE_62383 | chr5:156965587-157041636 | Tonsil |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 157038022 | 157039894 | chr5 | 157038446 | 157039675 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH05I157610 | chr5 | 157037349 | 157041259 |
|
Enhancer Sequence | CAGAAAATTA GGAAAAGCCA ATTCAAATAA TCTAGAAAAC CGAAAGAGAG AACAAATACA 60 GCACAATAGG CAAAGTAAGC AGTAATATGG TTTTTCCTTG ACATTTGTAA GAATTCTAGG 120 CCTTTTATTT AGCTTCCCAC AAATTCACTG ATTCATTCTG TGGCATTGGC CGGGTTCTTC 180 CCATCTCTGG CCCTGTTTTC TATCTGTGGA AAGCAGATGC ATGAGTTGGG CTAGGTCAGG 240 GACGGCAAAC GACTTTTATC TTGAGTACGA ACCCCTTATC ACTGCCCGGG ACTGCCCAGA 300 CCACCTCTGT GATGAGAAGG AATGTCTGAT AGAAGGTGAG AGCTCTGTGA CCCACTAACA 360 ATGTCTGCTA GAGACATGAG AATGAGGAAT GACCTAGAAA GGCTATCCAC TTCCTGTATA 420 CTCCATAATG TAAAGGGCTC TTACAACTCT ATGAATCTGG CACATCTTTA AGCAAAAATA 480 TTAATCTGAA TTTGGAAAGT CATAGGGGTT GGGGGTACCT AACTACATGT ATTCATTTTT 540 GGTTAGGTTG CACTGAATGA CTAATTTTCC ATCTTACTTC ACAGACCCCA AGACATAACT 600 TAGGATTTAC TAAAGCAGAA AATGGCCATG GTGGTGGTGT CTCAATTGTA TTTGCACCCA 660 TTATGTCCAA GCCCAAGGAC AAAGAATAGA TCTGCAGCTG TTGTTTCAGC CTCTTCAACC 720 TGAAACAATC TGAAAGCCAC AGCTGTTGCA GGCATAAACC TGATCCTGGC TTTGTCCTTG 780 GTTTATGTCT CATGTTTTGG GGAACTCCGA AAGCCACTCT ACTGGGGTTG ATTCAGAGAA 840 GGCCACATTT ATTCATTACC CTCCTGGAAA GCAGAAGTGC TAAATGCACA TTTGTTAGTG 900 GACTTTCCAG CATGGAGTGG GATCCATTCC TGTCTTGACT CAAGGCCCAC AGAGGAGAGA 960 TGACATGCCT AAAGTCACGC ATGAAGTTCA ATCTACACCC AGCTTTGCCT GCAGGCAAGC 1020 AAACATGGAT TCTTTGGTAA AAATCCACAT CAGGTTGTCA GCAGCTTGTT ATTTGGAGGA 1080 AGGGGCAGTC TGAAGGGCTT GACTGTATCT CAGCTGAACC ACACTAATCT ACCATAGCTT 1140 CCACAGAGAA CAGCAGGCTG TTTTCAGGGA TCTCAGCAAC AGCTGTGCCT TCAAACCAAG 1200 ACACTTCAGA AAAATGATCC GAAAGTGGGC CGGGTGTTTC AGCAGGATTT GGTGGGACTT 1260 TCCTACTCAA ATGGCCCTTT GTGTGCTTTT AAAAGACAGG GCATTAACCT CGTGCGTGGC 1320 TAAAGCATGA TGGATGACTT GGAATTCTCC ATTTACATTT GGCTGGTGGC CACAGAGGAA 1380 CCGTCAAAAC GCCTGGGTAT CGGATGGACA GTACCTGGCT TGTTCAGACT TGTTTCTGAT 1440 GGAGTGAGTG GATCCCGAGG CTTTTGCTCT GCCCAGGTTT GATAAACTAA ACATGGCCAG 1500 GCTGTTAGAA AGCTGACTCC AGGGTTCCTC TCACTGCAGC AAAATTCAGT GTCCTGAATC 1560 CATAGCCTCT TTAATCATCT TTGTTTATAT TCAGCATCTT TATCTACTTC AGGGTTACTC 1620 TGATCTCTGC CCATTTGTTG CAAGATGTGT GTGGTCCTAC CCAAGACTTG GGCAGCAGGA 1680 GCACAGGGCC TGTGCTCATG TAGCTTCTAC CCAGCTCCAT GAAATCACCT GCTTGATCCT 1740 TTTACCTTCT CAGTAAGATG CTTGGCAAGT GAGAGTGAAT CTGGATCCGT CAGTTCTCCG 1800 GACAATCTTG TCAGGCCAGA GGGAGTCAGA AGTTGACCTT CTGCACCATG CTGGCACCAT 1860 TATGTGAGAG TATGCAGCAC TCTCAGGCAG GAGCTAGCTA GCGTAAATTA TTAGGTTCTT 1920 TTCTGGCAGA CCTGGGTCCT GCTCTTCCGT TTAAGAGGAG CTGTTTACGT CAATTGCTCC 1980 TCACTGGGCC TCAGTTTGTT CACCTTTCAC TTGTGTTTTT CATGAAGCTC AAAGGAGAAA 2040 GCAAAGTGTT CTGAATGACT TTATACAAAC ATGAGGAGGT GGTAGTGGCC AGTACCCTCC 2100 TAACAATTGT CTCATCACAT CTTGAGGAGA GAGAGAAGCT AAACACTAGT GCAAGTGGAT 2160 ACTTAAGTAA GATAAACTTA TTTCCCTTCT AATCATTTTT 2200
|