Tag | Content |
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EnhancerAtlas ID | HS051-07395 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr13:47241840-47242960 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr13:47242532-47242553 | CCTTTCTTTCTCTTTTAGTTA | + | 6.09 | IRF1 | MA0050.2 | chr13:47242227-47242248 | AGAAAGAAAGGGAAACTGAAA | - | 6.74 | IRF1 | MA0050.2 | chr13:47242233-47242254 | AAAGGGAAACTGAAACCCATC | - | 6.97 | IRF9 | MA0653.1 | chr13:47242235-47242250 | AGGGAAACTGAAACC | + | 6.02 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_14324 | chr13:47241650-47242893 | CD34_Primary_RO01549 | SE_26329 | chr13:47241821-47242908 | Duodenum_Smooth_Muscle | SE_30455 | chr13:47241764-47243668 | Fetal_Muscle | SE_54689 | chr13:47241818-47243170 | Stomach_Smooth_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr13 | 47242087 | 47242800 | chr13 | 47242224 | 47242549 | chr13 | 47241928 | 47242851 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I046664 | chr13 | 47238537 | 47243788 |
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Enhancer Sequence | TTTTCACAAA TAGGAGCACT CGTAACACAT ATCCAGGTCA CATTTATCAT TTTATAATGA 60 TGTTTCTTTC CTGATGATAA AAGCACTTGT AGAAAGTTTG GAAAATACAT CAAAGTATAA 120 TAATGGAAAT AAAAACCATC CATTGTACCT ATACCCGAAG AGGAGTACCG ATAGTATTTT 180 GGTGTATTTC CATTCTGTCT GTCTCTCCCC CTCACATACA CAGATACATG CATGTCTATA 240 AATACACTCA CACAGGAACA CAGCTTCTGA AACTTTATGC ATGTGTGTGC AAACACACAG 300 CAGTTTTATT AAATAGTTAC ACTGAATGAC ATACAGATTT TTAGATATTT CACTCTGTGG 360 TTGTTGGCTT CAACACCAGA AGGGCAGAGA AAGAAAGGGA AACTGAAACC CATCTGTCTT 420 TTTGCTTGGT AGCAGGAAAA AGGGGCTTTT TGTGGGGGAG GAGATTGAAA TAAATGGCTG 480 ACATATAAAT AAGGATGGTT CGTAGATTTT ATTTATCTAG TATTTTCCAT CTCCATGAAA 540 ACTAAGCATT GATGATAGAA AGTTCAGAAA CTTCTGGGTA GAGACCCTCT TCTTGTAGAG 600 CAGAGATGAG ACATCAACTT AGACTTTTTT GGCTGCTCTG TGGAACTAAA CCCCTCTGGG 660 CTGCAGTTCC ACTTTGCCAG AAGACCAACT TTCCTTTCTT TCTCTTTTAG TTAGCTCTCT 720 TGCAGATACC AAAACAGACT TAAACTGTAG CAACCCTTGT TTTAACAAAA GGAAGCTGAG 780 TCAAAATGTT GGAAATGAGC CCGGTGGTTT TGTGAGTTGC AGCAAAATTA TCTTCCCCAT 840 CCCTACTGCA ATGGATGAAA TGATGCCTGT GTGGTGCTGG TTGCTTTGGT CCAGCTGAGT 900 TTCCTGCACA CATTGTCAGG AGAGGGCAGT TGGCACCAGC TTCCCGTTGC TATTGGTTGT 960 GCAGGATGTG CTCTCCATCT GCCTCCTGGC TGGCCGAGGG CTCAGCTTCT AAGTGGCGGT 1020 GGCGGGGTGG CGGGGTGGCG GGGGGACTTT GATGGCATTC CTTGTGTTGA ATAAAGTTGT 1080 CTCTTTGAGA ACTGCCCATA CCCTTATTTT TTATTTTTTA 1120
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