Tag | Content |
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EnhancerAtlas ID | HS101-35747 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:138037430-138039520 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr5:138038310-138038331 | CTTCAGTCTCAGTTTCATTAT | + | 6.11 | Nr2f6(var.2) | MA0728.1 | chr5:138039419-138039434 | GAGGTCAGGAGTTCA | + | 6.22 | Nr5a2 | MA0505.1 | chr5:138037798-138037813 | GAGTTCAAGGTCAGG | + | 8.25 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_29550 | chr5:138037357-138039457 | 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 |
GH05I138701 | chr5 | 138037559 | 138039281 |
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Enhancer Sequence | CTCCAATCTC CCATTACATC CTCATCTCCA TGCAGTGTCC AAAAGCAGAG AGAACAGTGC 60 AAACTCGCTC CTTTTCAGAA CAAGGCAACC CTTCCCACAA CCCTGCACAG ATTCCTCTTC 120 ACATCTCATA GCATAAGAAA ATTACACAAC ACGCCCATTC CTAAACCAGT CATTAGCAAA 180 AGGAATGGGA TTACTAAGAC TGGTTTAGAG CTGGGCAAGG GAGAAACCTA GCTTCTGTAG 240 AACTTTAGTG AAGAACCAAT GTTCTCCATT TCTGACAAAA ACCAGGCTTC TGTGAGCAGA 300 GTGCAGTGGC GTGTGCCAAT AATCCCAGCT ACTCAGGAAG CTGAAGCAGG AGGATTGCTT 360 GAGCCCAGGA GTTCAAGGTC AGGAAAATAG TAAGCATGGA AAAAAAAGAA AGAAAACACA 420 AACCCCCATT CAACACTGTA CTGGAGGTCC TAACTAGTGA AATAAGGTAA GAAAAAGAAA 480 TAAAAGATGT ATATGTAAGA AAAATAAATA AATTTAAAAC CCAGGCTTCT GGAAGCAAAA 540 TTAAGCTTCA TTAAGCAAAG AAATGGGAAA GGCCTACCTA TAAGTAGGTG ATCAGGAGTA 600 TCAGCCACAG GAGGTCAGTG TGGCCAGAGC ATTGGTGTAA GAGGAGGTTA TAGAGGTGGA 660 ACTGAGGGAT GGCAGAGCTT GCTTTAGCTT CTTTGAATGC AGTCTTTCGA ACTGGATAAA 720 TCCCTAAGGG CCTTATCCTT ACCAGGAACC CCCTCCAGCA TCCCCCGCTC TCCAGGACCC 780 ACCCCACCTC TGGGTGAGGA GCCATGGAAA GACTGCCCAG CTCAGGCAAC AGACACCGAC 840 TTTAATACTA ACTGATGACA CTGGGTGTCA CCTTTCCTTC CTTCAGTCTC AGTTTCATTA 900 TCCATAAAAA TGATGCAATA ACGTTTGTCC TGTTGGCCAT TCAGGGAGGT TGTAAGAATC 960 AAGTGAGAGC ATATCTGCAT GTCCCTTGAT GTGCCATGAT TATTATTATT GCTATAGTTG 1020 TCATTCATCT TACATGAAAA ACAAAAGGAT TTTAAGTTTT AAGTAGTCAC ATGCTCCAGC 1080 TCCCGGGAAG GCACATCTGT CATTTTGGAA AGCTGTGTGT TCTGAGGGAG TAAGGAGGGT 1140 ACCCTTGGGC TCTTTGTTCC CCAGACCTTT TCTCAGCACC TCCTGTGCCC CCACCCCCAC 1200 CCTACCAGCA GCCTTCTGTG CTTTGCATCA CAGATGTCCT TGGAAACAAG CTCAGCTGAT 1260 GTTCAATAAA ATGTAGGCTA AAGCTGGCTG AGTTATTATC CTTTTTTCTT GATAAAAAGA 1320 GTGGATGTAT TTTCATTACT GGCAGAGTGC TTTTAGCTAG TGTGGACAAT TAAGCCCTGG 1380 AAATGCAGCA ATCCATTTCA CACTGAGAGA AGATTTGAGC AGGACTGTCA CCAAAAATCC 1440 AGGAGGAGCT GAAATCATGG CCATGGTGCC CAACAATAAA AAGCCATAGA TATTTGGAGG 1500 CAGCCCACAG GGATTTGCCC CTCCGTGGAA TGTTGCTGTT GCTGGCTTGG AATGAGAGCT 1560 GCGTCCCCTG ATGCTTCTCC ACTGGCCTCA AGACCCTTCT TAGCCACCCT CTTCCTCATT 1620 CTCACCTCTC TTGGGCAGGC AGGCAGGGAG GAGCACCCTG TTATTGGCAG CAGCTCCTAC 1680 CAAACTTTGC CTTTTAGGTT CAGGCACCCT TCTTGGTTTT CTTCATGATC TCCTGATCAT 1740 CTCCTTCACC TCTGGAGACA CATTCTGTCT CCAAAGAATT GGACCTCTAG ACCAAGAGAA 1800 TTGTCCATTC CAAAGCTACT AGATCAATGA CGAAGTCCTC CTGTAGGGAA TAACAACCCT 1860 CCTGCCTCCT CTATCCTTCC CTTCTTTCTT TCTCTTGTTC ATTTACTTCT TTTTAAAATG 1920 GTGGCCCAGG CATGGTGGCT CACACCTGTT ATCCCCGCAC TTTGGGAGGA CGAGGTGGGT 1980 GGATCACTTG AGGTCAGGAG TTCAAGACCA GCCAGGCCAA CATGGTGAAA CCCCATCTCT 2040 ACTAAAAATA CAAAAAGTTA GCCAGGCGTG GTGGCTAATC CCAGCTACTT 2090
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