Tag | Content |
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EnhancerAtlas ID | HS101-28366 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr21:44092120-44093820 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr21:44092595-44092606 | AAACCACAGAA | - | 6.32 | ZNF263 | MA0528.1 | chr21:44093346-44093367 | CTCCTCTCTTCCTACTCCTCT | - | 6.18 |
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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 |
GH21I042672 | chr21 | 44092879 | 44095747 |
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Enhancer Sequence | GATATAAAAG CTTAATAGCT TATAAAAGCT CTAAAAATGA TTCACAGTCT AGGATAGAGA 60 AAATAAAAGG AATTTGAATT GGTTTATTTT CCTTTAGAGG AGCCTAAATC AATATTTATT 120 CTGAGTATGC AATCAGAAAT ATCAGTAATT TGAGAACAAG GCAAACAGAG CTGCACATCC 180 CGTTATGGCC ACGAGCCCAC CTCGCCTTCG TTCAGACCAC AGCTGAAGGT CTGACTTAGG 240 TGCAGCACGC ACCCCTGGAG CTGAGGGCCT GGAGCAGGGC CAGGCCGGGC TCTTCTCTCT 300 CTTGTCTGTC CTCGTCTGTG GGGGAATGAA GATGACACAG CACTCAGGAG GTCCTTTTCA 360 GGACCCAGAG TCACTGGGCT TTTAGGGCGT TTGGCTCTGG TTCTAGCCCG AGTGTGGTCT 420 CAGTCCCCAT TGGTGGTTGT GGTTGTGGCA TGGGCATCAT TAGTCACACA ACATAAAACC 480 ACAGAACGCA GAATTTGCTC ACCCTGGTTC ACACAGGAGC AAGCTTGGGC ACCAGCACCC 540 CCTGAACGCA TGCCAAAGGG CAGGTCCAGC TCAGTGCTGG GGTGTGGAGG AACCCACCTG 600 GGGCCTGCCT GCAAAGACAG ATGCCCTGCC GTGTTTAGAA AAAGAGAAAA CTGGCCTAAA 660 CCACAGTGAG GTCAAATGGA TCATTTAACC CGTCGAGTTT GGTTTCTTGT TCATCCGACG 720 CGGTTGATCT TATTAACGCA TATGTGTTTG TGTTGATGTG GCCTCCAGCT TCTGTCGCAC 780 TGTGGACACA GTTGGATGTG GCTGCTAATC AATGCGGGGC TCCGTAGGTC AGTGAGAGCA 840 ATCAGAGCCT GCTGTGCGGT GGCATCCCCG AGTTAAGACA GGCTTTTGTC CCATACTCTA 900 TTGAAACACC CAGAAATGCT GACATGTTGA AGTTAAGGCC ATGTGCCTTG GTGCTACTTG 960 CTTGCGAAAC AGCCTTTGAA GGAAAAAGGA GGAGGAGGAT CCATGAGTTT CAAGGGTCCC 1020 CTCCTGTAAT CACGGCTGCC ACTCAACGGA GTAAGTAATG TGTAGCGGGC CCTCTATCTG 1080 CATGACGAAT CCTCCTAACA TTCCTGTGGG CGAGGTAGGA TTTGTCTCGC TTTGCAGCCG 1140 AAGAATCAGA GCCTCAGAAA AGTTAAGAAA TCTTCCCTGG GTCAAGCTGG TAGGAGGAGG 1200 GACTGGAACT GAACTCACAT CTCCACCTCC TCTCTTCCTA CTCCTCTGCC TTTCTTGCAC 1260 CTAGAGCAGT GTACAACATC AACAACTGAC CAGGGCGATC CTAGAGGTAA GAGACAGCCG 1320 AATGGCACGG ACCCAGCCAA GCCCAGGCCT GCCCAGGTGG AACAGAGCCA GCTAGGAGCA 1380 TTCGGTAGCA GAGGTCAGTC CGCTGATTGA CTGTTCTCAC TTCCAGGCCC ACAGCCTCCT 1440 CCACCCTGAT GGTCTATGAG TCTAGTGCGG CCCTTTGCAC AATTTTAGCA ACTGAACCCT 1500 TTTCCTCACA GAATTGTGAT ACCGTCCTAA CATATGAAGC ATATATAAAC AGTTGGGCAA 1560 ATCATAATAG TTTCCATTAT TTCATAAATT TGCATTTGTG GCACCAAGGA GAGAATTAAT 1620 GGGAACAAGA GGGTTCTTGT GTGAGTTCCG CATTTGGATT TGGGGGTTCG AGGTGGCAGC 1680 TATAGGCTCA CATTAGTGTC 1700
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