Tag | Content |
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EnhancerAtlas ID | HS108-06222 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr10:99407990-99409480 |
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 | AGGCATGTGC CACCATGCCT GGCTAATTTT GTATTTTTAG TAGAGATGGG GTTTCTCCAT 60 GTTGGTCAGG CTGGTCTCGA ACTCCTGACC TCAGGTGATC CACCCTCCTT GGCCTCCCAA 120 AGTGCTGGGA TTACAGGCAT GATTCCCGGC TAATTTTTAA AAATTAGTGA CAGAGTCTTG 180 TGGTATTGCC CAAACTGGTC TCAAACTCCA GGCCTCAGGC AATCCTGCCT CATCCTCTGA 240 AAGTGCTGGG CTTATAGGCA TGAGCCACCA TGCCCAACTT TTTCTGTCTT TAAGTAGAAG 300 TATTTACCAG TTGACCTCAG CCCTGGTATT TTTCAGCCCC CAGTAGTAGT AGGAGTGTCT 360 TGGCCTCCTT TTCATTGAGG ACCAGCTTAC TGAACTCCAT AATGTGCCTC AGTTGAACTG 420 ACTGTTGCGT TCTGGGACAT GCTTCAAGTT GCCTTTTGGT TTCCCTGTCC AGGGTCCGGA 480 GGGTTACAGT GGACTCGTCA GTCATTCTCT GAGTTGTGAG CCTGTTGCTA CTGCTGCTTT 540 GTTATTCAGA GGCTGGGGTT CCAGGGGAGC AGAGACAGAG AAGACTGCTG AGGACTCTAG 600 CTAGCTGCTT TGCATAAGAA AGTAATTCTG AAGACTTATG ATGTGAATAT ATGCATTTTG 660 CATTTGCCAG TAAATAAGTT AGTTTGTCTT TAAGAATAAA TTGATTCTTT TTGGAGGGAG 720 AAGGAGGAGT TCTGTATTTT TCTTGTCCTC TCAAATCCTT GGAAGGCATT TTTAAAGGAG 780 CTGGCTTCAA GATCGACCAG TTATTGTTAG CGACATGGAC CTAGCTAGTT CCTAATATGA 840 GTACTGAGTT GGTAAAAGCA GATGGGTGTA TGTTGTCTGC TGTGACCTGC CATTCAGGAA 900 GTGACACCCA CAGAAAAATA TCTTATGACC CAGACTAGCT TGAGTAGGCT GTGGGGTGAG 960 GGGACAAGGA GAGTCATATG ATATGAGGAT GAATCACTTG GATAGCATAT TTGCTTTTTT 1020 CCTTTGAATT ACCAGTTTGG GGACTGGAGG GAATTAGATG AATGTAAAAC AACCTCAGAG 1080 GGCTGACTGG CCTGTTGAAG AAAACACTCA GGAGGGAGGG CCATAGTTTC TAGGCATCCC 1140 ATATTTCCAA AGACCTTAGA AGATTAAGTT ACTGTCTGCT ATAGAAGATG GATTTAATCT 1200 GTGTGGCATC TCATGTCCTG GTTTCTTGCC TATCAGAATT ACTTAAGAGA GCTTCATTCT 1260 AACCAAGTAG CAGAGTCTTT TTCCTGCTGT GATTTTTCTC TTTGGATAAT AAGGCTGCGA 1320 GAGGAAATCT CTTCATCATT GATGAAGGAA TTTCCTTAAC CTCATTCCAT AATAGATTTT 1380 TTTTTTTTTT TTTTTTTTTT TTTTTTTGAG GCAGAGGCTT GGTCTTGTCA CCCAGGCTGG 1440 AGTGCAGTGG CGTGATCTCA GCTCACTGCA ACCTCCGCCT CCTGAGTTCA 1490
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