Tag | Content |
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EnhancerAtlas ID | HS133-23884 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr4:38871500-38873000 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr4:38872697-38872718 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 38872074 | 38872309 | chr4 | 38872350 | 38872435 |
| Enhancer Sequence | AACTTGAAAG ATGAAGGCAG TCCTTTACAT TTAATAAATT TAGATTTATG AAAAACTTGC 60 AATCTTGTCC TCATTTTTCT CTATCATCAC AGACTTGCCC CAGTCCTGCA GGTGGAGTTT 120 GGAAAAAAAA GCATCCAGAT CAGTTTGTCC ATCCTAGCTT TACAGAGGAG CAGGTGTAAG 180 CACAGTGAGG ATCAAGTTGT GTGCCCACAA AGGGATACTG GGACCAGAGG CCACATCCCT 240 TGACGCCTGC AGGACACAAC TCTTTCCACC TCAGAATACC ATCGCTCCCA CCTCTCATCA 300 TTCCTCCATG CAGCCTCATG TCCTGGCCTC TCAGACACCT GTCCTGAATC ACTACAGTCC 360 ATCGCTGATG CTTGGACATT TGCACATGCT CTCATCCCAC CAGGCCTGAA TCACCACATC 420 AAAGACACTT TCAAGATTCT CCCTTGCACA GGGTCAGTCT AGTTCAGGCA CATCTGTCCT 480 TGATTTGCTG TGCTGTTTTG CATCACTTTT TAACTGTTTT GTGTTAGCTC CTCAAACAGA 540 TGATTGATTT CTGAAGGATA GTGACCATGT CTTCTGTTTT ATACTTATTT TTGGAGCTGT 600 GATGTTGCTG CTTAAATACC TTGCATAGTT CTGGGAGCAT TTTAGGTGAT GAATGAATTT 660 ACTCACGAAA AACTAACTTA TTCCCAGCCC ACAAAGGCTT CTTTATATGC CACCCTTCCT 720 CTCCTTAGAG TTTCCTGAAG CAGCCTCCTT GTTTCTGTGG GTTGAGTCTC CCTAGCCTCC 780 AGTCCACGAG ACATGGCTAC AGTGATCAGT GTTCCTAACC ATAAATCAGG AAAGGTTTCT 840 AAGTCTGGCT TATGGAACAC CCAGACGGAG ATGGAAACCG TCCCAGGAAA CACAGTGCTT 900 GTCATGACTG TAATCCTGGT GGACTCCAGC AGCCCCTGCT CAGAAACAGT TCTGTATTTC 960 AAACACACAG TTTCTAGTGG TTTCATACAA AAGGGTATAG TCTGAAAAAT GATTACATTT 1020 CCCCCATCAT GATAGCATCC ACAGTCGATA AAGTTCTACC AGAACAACCA AACAAAAAAT 1080 AATTTTTTTT CGTTTTGATT TGGGGAAAAT TAGACCTGTA ACAAGTAGAG ATAAATATGG 1140 ATTAGAGATA CACACAATTA GAAATTGAAT TAGAGCTGAT CTTGCATGGC TTTCTTTTTT 1200 TTCTTTCTTT TTTTTTTTTT TTTTTTTTGC GACAGGGTCT CACACTGTCA CCCAGGCTGG 1260 AGTGCAGTGG CATGATCCTG GCTCACTGTA GCCTCTGCCT TCCAGGTTCA AGCAATTCTC 1320 ATGCCTCAGC CTCCAGAGTA GCTGGGATTA CAGGCACATG CCACCATGCC CAGCTAATTT 1380 TTTTGTATTT TTAGTAGAGA CAGGATTTCA CTCTGCTGGG CAGGCTGGTC TGGAACTCCT 1440 GGCCTCAAGT GATCTGTCTG CCTTGGCCTC CCAAAGTGCT GGGATGTGAG CCACTATGCC 1500
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