Tag | Content |
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EnhancerAtlas ID | HS148-02613 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr10:99408090-99409440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr10:99409274-99409285 | TGCTGTGATTT | - | 6.62 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28147 | chr10:99406936-99409463 | Fetal_Intestine | SE_28882 | chr10:99406819-99410069 | Fetal_Intestine_Large |
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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 |
GH10I097647 | chr10 | 99407084 | 99413128 |
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Enhancer Sequence | CACCCTCCTT GGCCTCCCAA AGTGCTGGGA TTACAGGCAT GATTCCCGGC TAATTTTTAA 60 AAATTAGTGA CAGAGTCTTG TGGTATTGCC CAAACTGGTC TCAAACTCCA GGCCTCAGGC 120 AATCCTGCCT CATCCTCTGA AAGTGCTGGG CTTATAGGCA TGAGCCACCA TGCCCAACTT 180 TTTCTGTCTT TAAGTAGAAG TATTTACCAG TTGACCTCAG CCCTGGTATT TTTCAGCCCC 240 CAGTAGTAGT AGGAGTGTCT TGGCCTCCTT TTCATTGAGG ACCAGCTTAC TGAACTCCAT 300 AATGTGCCTC AGTTGAACTG ACTGTTGCGT TCTGGGACAT GCTTCAAGTT GCCTTTTGGT 360 TTCCCTGTCC AGGGTCCGGA GGGTTACAGT GGACTCGTCA GTCATTCTCT GAGTTGTGAG 420 CCTGTTGCTA CTGCTGCTTT GTTATTCAGA GGCTGGGGTT CCAGGGGAGC AGAGACAGAG 480 AAGACTGCTG AGGACTCTAG CTAGCTGCTT TGCATAAGAA AGTAATTCTG AAGACTTATG 540 ATGTGAATAT ATGCATTTTG CATTTGCCAG TAAATAAGTT AGTTTGTCTT TAAGAATAAA 600 TTGATTCTTT TTGGAGGGAG AAGGAGGAGT TCTGTATTTT TCTTGTCCTC TCAAATCCTT 660 GGAAGGCATT TTTAAAGGAG CTGGCTTCAA GATCGACCAG TTATTGTTAG CGACATGGAC 720 CTAGCTAGTT CCTAATATGA GTACTGAGTT GGTAAAAGCA GATGGGTGTA TGTTGTCTGC 780 TGTGACCTGC CATTCAGGAA GTGACACCCA CAGAAAAATA TCTTATGACC CAGACTAGCT 840 TGAGTAGGCT GTGGGGTGAG GGGACAAGGA GAGTCATATG ATATGAGGAT GAATCACTTG 900 GATAGCATAT TTGCTTTTTT CCTTTGAATT ACCAGTTTGG GGACTGGAGG GAATTAGATG 960 AATGTAAAAC AACCTCAGAG GGCTGACTGG CCTGTTGAAG AAAACACTCA GGAGGGAGGG 1020 CCATAGTTTC TAGGCATCCC ATATTTCCAA AGACCTTAGA AGATTAAGTT ACTGTCTGCT 1080 ATAGAAGATG GATTTAATCT GTGTGGCATC TCATGTCCTG GTTTCTTGCC TATCAGAATT 1140 ACTTAAGAGA GCTTCATTCT AACCAAGTAG CAGAGTCTTT TTCCTGCTGT GATTTTTCTC 1200 TTTGGATAAT AAGGCTGCGA GAGGAAATCT CTTCATCATT GATGAAGGAA TTTCCTTAAC 1260 CTCATTCCAT AATAGATTTT TTTTTTTTTT TTTTTTTTTT TTTTTTTGAG GCAGAGGCTT 1320 GGTCTTGTCA CCCAGGCTGG AGTGCAGTGG 1350
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