Tag | Content |
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EnhancerAtlas ID | HS047-24378 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr3:123128050-123129470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr3:123128450-123128463 | AGGAGCAGCTGCA | - | 6.15 | ZNF263 | MA0528.1 | chr3:123129158-123129179 | TCCCCCTCCTCCTCCTCCCCC | - | 10.05 | ZNF263 | MA0528.1 | chr3:123129009-123129030 | GAATGAGAAAGGGAGGGAAGG | + | 6.09 | ZNF263 | MA0528.1 | chr3:123129184-123129205 | TTATCCCCCAATTCCTCCTCC | - | 6.28 | ZNF263 | MA0528.1 | chr3:123129193-123129214 | AATTCCTCCTCCTCCTCCTCA | - | 6.38 | ZNF263 | MA0528.1 | chr3:123129196-123129217 | TCCTCCTCCTCCTCCTCAACA | - | 6.6 | ZNF263 | MA0528.1 | chr3:123129190-123129211 | CCCAATTCCTCCTCCTCCTCC | - | 7.01 | ZNF263 | MA0528.1 | chr3:123129187-123129208 | TCCCCCAATTCCTCCTCCTCC | - | 7.21 | ZNF263 | MA0528.1 | chr3:123129152-123129173 | GTTCCATCCCCCTCCTCCTCC | - | 7.29 | ZNF263 | MA0528.1 | chr3:123129155-123129176 | CCATCCCCCTCCTCCTCCTCC | - | 8.95 |
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| Number of super-enhancer constituents: 15 | ID | Coordinate | Tissue/cell |
SE_00289 | chr3:123129326-123132888 | Adipose_Nuclei | SE_01550 | chr3:123127988-123129579 | Aorta | SE_03867 | chr3:123128825-123146146 | Brain_Anterior_Caudate | SE_04971 | chr3:123128740-123149524 | Brain_Cingulate_Gyrus | SE_05846 | chr3:123127963-123154367 | Brain_Hippocampus_Middle | SE_07929 | chr3:123128250-123134602 | Brain_Inferior_Temporal_Lobe | SE_26038 | chr3:123127784-123136151 | Duodenum_Smooth_Muscle | SE_26748 | chr3:123128718-123129516 | Esophagus | SE_40589 | chr3:123127759-123154640 | Left_Ventricle | SE_42153 | chr3:123127874-123129586 | Lung | SE_46690 | chr3:123128738-123128936 | Ovary | SE_47869 | chr3:123128079-123128765 | Pancreas | SE_47869 | chr3:123128797-123129425 | Pancreas | SE_48554 | chr3:123128036-123129657 | Right_Atrium | SE_54494 | chr3:123127664-123146810 | Stomach_Smooth_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 123128274 | 123129234 | chr3 | 123128765 | 123129151 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I123409 | chr3 | 123127455 | 123134665 |
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Enhancer Sequence | TTTAGAAAAG TTTAACCCTT ATAAGGGTCT GCTTTAACTA TATCCACTCA ACACCTAGTT 60 CCTCTATGTG CTAGGGGCTG TGCTAGGTGC CATGGGGGCC CCCAGGGATT GGTAAGAGTG 120 AGTCCCAATA CTCCAGGTGT GTACAGTCGC AGGCCATGAA ACCAGGTAGC ATGTGGGGAA 180 AAAGGACAGA CGGCCCAGCA CATGCTAGTT CTCAGGGTGG CCACTGGAGA AGGTATCCTT 240 GGAGTCAGGG TCTAAAGGTG GGATGCAGCT TTCACAGGTG GAAAGGATGT GTTCCTGCTA 300 ATAGTCCTGT CCAAGCAGCA CAGATAGGTA AGGGAAGCAC CACCAAAAAT CCTCAACTGA 360 TTATCTAGCA CAGTGGTTCT CCAAGTGGGA TATCCAGAGC AGGAGCAGCT GCAGCATCAC 420 CCAGGAAGCA GCTAGACATG CAAATTATTG GGCTCCACCT CTGACCTTGT GACTCAGAAA 480 CTCTGGGAGC CCAGCAAGCT CTCCAGGAGG TTAAGATGCC CACTCATGTT GAGATGCCCC 540 TCTTGCACCT CACCTGCTTC CTTAACAGAG GCCGGGCAGA AGGTAGAAAC TGCCCCAGAG 600 ACATTCCCTC ACTCACCGGC CCCTCCCACC CTCCAAGCCC CAGTTGGATG AGCTGAGAAA 660 GTTCCCTGTG GTTAGAGGAG CTAATCTATC ACCTGGATAT AAATTAACTT GCCCTCTCTC 720 GTCACCAGCC CACTGACCTG GGAAAGGCAA ACACGCAGCT GGCAGGGAAA GAGCAGTAAT 780 AAATCTCTTT TTCTACAGGT CCTCCCACAC CCACTTCCCC AACTGAGACC TGTGTTCCCT 840 GAGGCAGTGT GGCCCCATAG CCCTGAGGTC CCTCTGCTCT CCCACATGAG CAGGTGCTGG 900 ATCCGGTCAA CCCAGTGAGA GGCCCCCATC TGCCCTCAGG GCCTCCACCA GAACTAGGAG 960 AATGAGAAAG GGAGGGAAGG ATGGGGGCTG GAACACAGCT CATCACCCTT AAGGATGGCA 1020 GAGTGACTGG AAGCTTCCCT TGTAGAACTC CTCAGGAAAC AGCCCACAAA GACTCCCTCC 1080 AGGGCAGCTC TGTCTTGGCA GAGTTCCATC CCCCTCCTCC TCCTCCCCCA ACCCTTATCC 1140 CCCAATTCCT CCTCCTCCTC CTCAACACAG CAGCCTGGGG CCACCCCGTA CCTCCCAGGC 1200 ATAAGTAGGA ATGGTAGAGC CATATCCCAA GGTGAACTGC CTGTTGGGGA AGGGCTAATC 1260 TCCTATTATT CCAACACCCT TGGCCACATC CTGCACTCTG TCTGCCTTTG GAATGACCAG 1320 GTGAAAACCA ACATAACGTC CACCTTAGAA AGCTGCAGTA AGAATGAAAT CTAACAGGAC 1380 ACATAAAGGA CATAAAATAA AGGCTCAACA ATGGCAGCTC 1420
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