Tag | Content |
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EnhancerAtlas ID | HS012-20229 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr5:149989070-149990290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr5:149990197-149990207 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr5:149990197-149990207 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr5:149990197-149990207 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr5:149990197-149990207 | AACAGCTGTT | - | 6.02 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00123 | chr5:149988443-149996761 | Adipose_Nuclei | SE_01549 | chr5:149989048-149990225 | Aorta | SE_06402 | chr5:149988927-149990383 | Brain_Hippocampus_Middle | SE_08263 | chr5:149988978-149990399 | Brain_Inferior_Temporal_Lobe | SE_23666 | chr5:149989078-149990282 | Colon_Crypt_1 | SE_26296 | chr5:149989147-149992534 | Duodenum_Smooth_Muscle | SE_27146 | chr5:149989116-149990290 | Esophagus | SE_27995 | chr5:149988076-149994045 | Fetal_Intestine | SE_29147 | chr5:149988185-149993250 | Fetal_Intestine_Large | SE_29818 | chr5:149989311-149990661 | Fetal_Muscle | SE_31661 | chr5:149989262-149990270 | Gastric | SE_40596 | chr5:149989004-149997010 | Left_Ventricle | SE_42134 | chr5:149988999-149990374 | Lung | SE_46676 | chr5:149989319-149989558 | Ovary | SE_46676 | chr5:149989564-149990152 | Ovary | SE_48061 | chr5:149987456-149990272 | Psoas_Muscle | SE_48556 | chr5:149989028-149990362 | Right_Atrium | SE_49445 | chr5:149989259-149989610 | Right_Ventricle | SE_49445 | chr5:149989611-149990165 | Right_Ventricle | SE_50806 | chr5:149989183-149990245 | Sigmoid_Colon | SE_51080 | chr5:149987244-149996627 | Skeletal_Muscle | SE_52506 | chr5:149989033-149990362 | Small_Intestine | SE_54988 | chr5:149989204-149992386 | Stomach_Smooth_Muscle | SE_65294 | chr5:149989219-149990181 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 149989391 | 149990000 | chr5 | 149989582 | 149989693 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I150608 | chr5 | 149988419 | 149996410 |
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Enhancer Sequence | GGTCTCGAAC TCCTGACCTC AGGTGATCTG CCCACCTCGC CCTCCCAAAA TGCTGGGATT 60 ATCGGCGTGA GCCATCATGC CTGGCTGGTT AGGCATTTTC TGAATTTTTA GTCCTTGAAC 120 CCTTTCTGCA ATGCAATATT TGGGAGCCCC AATGTATGCA ACAGATAAAA AGCAGTATGT 180 TATCAGCATA AGTTTACTAT AGAAACCGAA ATCATAGTAT CCGTCTCAGT CTCTTGTTTA 240 AACTGGGGGA CAGGGTGAGG GGGCACTGTG AATGTGGCGG GGGGGGGCAG TGTGGAGCAG 300 TCTCAGAGCC AGGGCCCTGT GTGCCAGCCC TCTCCCCATC TGCTGACTGC GTAGCCTTGG 360 GCAAGTCCCT CCCCATCTGA GCCCCCATTT TCTGGTGTGG CCAAGGGAGA CTGGACTTTG 420 TGCAGAGTGG CCTCTGCCCT GCCACACCCC TGCCTGACCT CAGCCAGTCT CAGCCCCGTA 480 TTTATAGCCA TGACTTCAGT CTCCCCAGTT CCTCTGAAGC TGGTTCCCTG GCCCATGTAT 540 TTATAAACCC AGCAGGGCAG AAATAGATGT GACGTACTGG GGACTTGGCT GGTTCTGTGA 600 GCAGGCTGGC TTCAGTGAGT CCACTTGGAA CAGGCTTGAG TGCCCCAGCA TCCTGGGTGC 660 TGAGTTCCAC AGGCAGTCTA AAGCTGGAAG AGCATTTTGA GACCCCAGGC CCAGGCTTGT 720 CATTGTGCAG GGAGGTCACC AAAGCCCAAG AGTGGAGGCA TGTGGCCACA GTCACAGGCA 780 CGGCAGAGCC AGAGCCAGAA CAAAGGACTC TGTGCTGTGT GAAATGGCCT CTCCCCAGAC 840 CCTCAGAAAA CCTCCAGTGA CCACGCCAGG CCACAGACAC CGGTCAGGTT CCAGCTTGGT 900 CATTTTCCTG CTCTGGGATC ATGGGCACAG ACTCACCCTC TGTGAGCCTC TGCTTCCTCA 960 ATCTGTTAAC TGAGGGATAA CAGTAGGTGC CTGCCTCATA ATGTTATTGT GAGGAAGAAA 1020 CAAGAAACAA GATTGATACA GTGCCCAGCA CATGCTCAAT ATTCAATACG TGGTAGCTCT 1080 TGTAATGCCC TCAGTCACCA CTTCACAAAA ACAATAATTA TAATAACAAC AGCTGTTTCT 1140 ATTGAGCATG TACACAGGTT ACCTTATTTA ATCCTCACAG CAATATGATA TCATTATTAT 1200 TGTCCTCAAA CTCATTGCAT 1220
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