Tag | Content |
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EnhancerAtlas ID | HS133-28386 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:44769300-44770150 |
Target genes | Number: 15 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr7:44769624-44769639 | TGCCCTCTGCCCTCC | - | 6.45 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 44769400 | 44770009 | chr7 | 44769618 | 44769736 |
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Enhancer Sequence | TCCTAATTGT TTTTCTTTTT TTTACAGTCA TGTCCATCTT TGAGTGGTGC CTTTTTTTTT 60 AGCCTTTTTT GCATACTCAC AAACCAATCA GCATGCAATC CCCCATTATG AGCCCATAAG 120 CCCCAGACTC AGCCACACTT GTGGGTGGGG GATCACCCTC CCCAAGTCCC CTCTCAGCTG 180 AGAGCTGTTC CATATGGCTC AATAAAACTC TTCTCTGCCC TTCTCACCCT CTGGTTGTCC 240 ACGTAACATC ATTCTTCTTG GATGCAGGAC AAGAACTCAG GACCTACTGA ATGGCGGGTG 300 CCAAAGGAGC TGCTCTAACA CTGTTGCCCT CTGCCCTCCA CTGGCTCCAA GCAGATGACC 360 CACGTGACAG GAAGCCACAG TTGAGGCCAG GCCAGCCCTG GAGCCACGGG CCAGAGTGGG 420 GCAGCGGGAC TCAATGAGCT GTAACACAGA CTGGCTTAAA CACGCCCCCA ATCCCCCTGT 480 TTGAAATGCT GTGGGCGATG GGAAGAGAAG AGCTATGTCC CTTCTGGGGG CCTAGACCTC 540 GGGGCTCCCC AAGCCAAAGC TGTAGCACAC TGTAACACCT CCTGTGGTGG GCTTCAGGGT 600 CGCTGGCGTC TTGATTTTCT CAGGTGCCAC TGCGTTCCCC TTGTCCAGGC ACTGGTGCCC 660 AAGGCAGGAG CAGGTCACAG CACCCCTGGC CCACCTGTTG GCTGAGTGCA AGCCAAGGGC 720 AGCCTCTGGG CTGCGTGGGT GGGGTACCTC CAGATGCAAG CCTGGAGCCA AGCAAAGCCC 780 TGTGAAGGGG GTTGCCAACC ACAGAGGTCT CCGGCTGGTG AAACAGCACC AAAAAAATCC 840 TGCATCACCA 850
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