Tag | Content |
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EnhancerAtlas ID | HS133-27153 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr6:53702310-53703780 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr6:53703636-53703647 | TGCTGAGATTT | - | 6.32 | STAT1 | MA0137.3 | chr6:53703350-53703361 | TTTCCTAGAAA | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH06I053837 | chr6 | 53702613 | 53703175 | GH06I053838 | chr6 | 53703281 | 53703430 |
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Enhancer Sequence | GTAAATTTGG TGTTATTATA GTTAGGAGTC CCATAGTTTT TCAGGAATTA ATAGCATTTT 60 TTACATTAGT TGTTCTCCAT TTGAATTTGT AACAATGGTT TATGTTTTCT CTATATTGCA 120 GAGGAGAAGT TTGGGCAACT GGGGGACAAT TGACTGATCC TTGGCCATAT AATAATAAAA 180 GGGGACCCAG CTCTTCTAGG ACTGAGATTT TCTTTGTCCC TTTCTAAAAA GCAGAAGGGA 240 GGTACTAACA CTTTACCAAA AAAGAAGGAA AAGAATCTTG TCAGAAATGG AGAATGGGAG 300 AACATTTAGC CAAATTAAAG GCTGTATCTA CTAAAAGCAA TGGTGGCTCT AAGAAGATGG 360 GTGTAGCATA ACAACCCGAG GCAATTTGGG TTCCTTTGCA TATAATTGTA CAGAATGTGC 420 TCTAAGTGGG TTAGTGAGCT ATAATCAAAC ATGGTAGAGT TGAAGAATGG TGTCTGTGTG 480 TTCTGTCACA TGGTTGCACT GCACTGAGGC TTCCTGCCAA GACAGCTACA GGAATTGTTT 540 TTCATGGGCT CTGGCTGATC TCAAAGGCAA GGCAGAAGGG TTTATAGCTT AGTGAGTTAT 600 TTTTCCTGAC TCTCTAAGGA AGCTGAATAT TTGAGAATTT AATACAGTTT CCTTGGCATT 660 GTGTTGATCT TTGGATACCA TATTAAGATC ACATCAGGAT AATGAGGGAA GGATTAAGGA 720 ATTACTGGTT TCATTTGGGA TCATGTCAGA TGGGGTTGTT TTTACATCTG GCATGTACTT 780 CCCAAGTTGA ATAAAGTAGT ATTTGTGACA GGCTCTAGTG GAGGATGCTG GTAACATGCA 840 GAACCAAACC TTAAATTTGC ATGCTGTTAT GACTTCTATT GGATGTGAGG ATTTGTAGGT 900 TATCGTTTCC ACAGATGTAA AGTGAACTTA TTATTCACTG TACATCTAAG TACCTTATTG 960 ACTTGATTTC TTGTCTTATT TCTGAATGGT CCCAGAATGT ATGGAGATGG TGATGGGTTT 1020 TGTAGTTTTG CTATTATGCC TTTCCTAGAA AACAAAGTGA GCTTTTCATG CTTGAGTAAA 1080 CACATTGATG TATTATGAAA CTGTCAAGAC TCTGTACAAT TGGCATAAGC TCAATTATTC 1140 AAATACGTGA CTCTATTGAA TGGCTTTTGT GCTGGCTGAT GCTTTAGTTC AGCCAGTATA 1200 AAGACATTTC AATATCTTTC CTTAAGAAAT TAAATCTCAA CTGCATGAGT AAAGAAATGC 1260 AAAGGATTAG TCCTGTAGTT GAGCACTTTC CTCATCATCT TGTATAGCTA ATTGGTAGCA 1320 TTCATTTGCT GAGATTTATA GTTCATTTTA TTTTTTAAAA AAATATGGTT TTTAAATTAA 1380 AAAGTCATTC ATGCATTATC TTTGTCACCC AACATAACTG CTTTTTTCTT CTTTGTTCTC 1440 TTCCTGTCAG TCCACATGCA CACATGCTTT 1470
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