Tag | Content |
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EnhancerAtlas ID | HS176-38976 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:151042570-151044060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6 | MA0677.1 | chr7:151043424-151043438 | TGACCTTTGTCCCT | - | 6.19 | Rxra | MA0512.2 | chr7:151043424-151043438 | TGACCTTTGTCCCT | - | 6.05 |
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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: 1 | ID | Chromosome | Start | End |
GH07I151345 | chr7 | 151042315 | 151044171 |
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Enhancer Sequence | ATCAATAATT AGCAGCATTA TAAATCTCCT TGGTAAATAA GATTCTGAAT TGTCAGGCAT 60 GACCATATAA ACTTTTGGCA TAACCAAAAG CATTAGTGGT GAGCGGGTAC CCACTTTTTA 120 CTAGGAACTG ACAACCTTAT TTTTGTTCAT TAATATTTTA TTCACATGAG GATGTTATCT 180 AATTTTTCAG GCATATATTT TTAATACCAT CACAGGATTA CATAACATTA TTTATCTGGA 240 ACTCATTTTG ACCCATTAGT GGAACAGTAT TGGTGCCAGT AAGTAATTGC ATTGTGTGTT 300 CAAAGTGACA GTGTCTTGGC TCATTCTCGG TCCTCCTTGC TATCATCATC TGCTGTGAAA 360 CAATTGCTCC TTTTTCCCCC AGTTTTTTTG ATGCTCTCAC TATCAGTGTT CATTTTTCCA 420 AAATAGGTTT TTTCTAACAG TTGTATCTCA GTTTTTCATG GCATCATCAG AAATGATATT 480 GTATGTAAGT GATGTTTCTA GAAACTGAAG TCTGCTTGCT TTTCTAAGCA GAGAAACAGT 540 ACTCATTTTT GCCAGAAATC TATCATACTG GAATTTCCTA GCATGTACTT CTCTGCTCTC 600 ATTCAGAGTA TCCTGAACAT GATGTAACAT TTATCAGGGA CTAAGGATTG TCATGAGGCA 660 TTAAATTGCT CTGTGTTGTG ACATAATGAT GTGCTTGGGA GGTGACAAAC TGTATTAGGG 720 TCCTAGTTCT TCTGTTTCTT CTGTTCCAGG CAGGCCTCAC TTTTTCTTTG CAACCCACCT 780 TCTGACCTTG CTTCTGAATT TATTGTTACA GTCTCTTGGT TTAGAAACTA GGTGTGGCAT 840 AAAGGAAAAA TATTTGACCT TTGTCCCTGG TTCCTGGCAG AGCCAAAACT CTTGGGATTT 900 CCTAAGTGGT AAGCATGATA GGAGCAACCT TTGTGCTCAT GAGGCTTGGT TGCCCCTAGA 960 TAGCTTCAGG ATGGGGCTGG TCACCAAAAG TACCAAGCCG TGATTAGACA CTTGAAACTT 1020 TCCACCCTCC CCTCCAACCT CTGGGAAGGG GAGATTGAGC TGATGACTAA TACTAATGGT 1080 CAGTGATTTA ATCAGGCCTG CATAATGAAA CTTCCATACA AACCCCTAAG TGACAGATTT 1140 TGGACAGCTT CCAAATTGGT GAACACATCC ACATGTCGGG ATGTACACCC CCAACTCCAT 1200 GGGACAGAGG CTTCTATGCT CAGGACCCTT CCAGACCTTG CCTTAGTACC TCTTCATGTG 1260 AATGGTTATT TGTATCCTTT GTAATGAACT ATATTCATAA GTATACCATT TTCTGGAGTT 1320 CTGTGAGTTG TTCTAGCAAA TCATGGAACC TGAAGGGGGT GCTTGTGTGA ACCCTCGACT 1380 TTGTAGCTAA GTCAGACAAA AGTATGGGTA ACCTGGGGAC CAGATACTTG GTAACTGGTA 1440 TCTGAAGTTA GGGCTTTTTT GTGGGCTGAG CCCTTAAACC TGTGGAGTCT 1490
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