Tag | Content |
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EnhancerAtlas ID | HS105-26033 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr14:103996650-103997640 |
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) |
ESR2 | MA0258.2 | chr14:103997319-103997334 | AGGTCACCATGTCCC | + | 6.96 | REST | MA0138.2 | chr14:103996936-103996957 | GGCGCTGTCCTAGGTACTGAC | - | 9.05 | ZBTB33 | MA0527.1 | chr14:103997440-103997455 | CCACTCTCGCGAGAG | - | 6.61 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_05960 | chr14:103992335-103997950 | Brain_Hippocampus_Middle | SE_23413 | chr14:103995501-103997086 | Colon_Crypt_1 | SE_24782 | chr14:103992179-103996793 | Colon_Crypt_3 | SE_54593 | chr14:103996750-104012040 | Stomach_Smooth_Muscle | SE_59458 | chr14:103984992-103996839 | Ly3 | SE_65682 | chr14:103991832-103996969 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH14I103530 | chr14 | 103996841 | 103996990 |
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Enhancer Sequence | GTTCCTCAGG CTGCCTCAGT TTAACGCAGA AATTGACACA AAGGTGGAGG TCAGAGCCTC 60 CAGCCTGCCC TTCCTACAGA CACATGTGGC TCCTCAGTTT CTATTTTCAC ATCTTTCCGG 120 GATGCTGACA GCAGGGAGTG AAGGTGGAGG CAGAGAAGCC CGTTAGGAGG CTGGTGCTGT 180 AACTGGAGTG AGAGGTGGTG GGAAATGGAC CAGGAGGAGC TGGGGAGGAC TGGTGCTCTA 240 GTGAGGGTCC TGCTTGCCTT GGTGGGGCGT GGCCAGCTTG ATGCTTGGCG CTGTCCTAGG 300 TACTGACCGT CAACCTCTAG TCCTCCGTGC TGATGGTGAA GCAGAGAGAG TTGCCCCTTC 360 TGGAAAGAGG CCAGGGCTAC CCCGAGGAGC TCACTGTAGG TGGGGAGCCT TCCCCATCCT 420 CATCCATGAT CAGATCCTCA CCTGCTACCA ATGAATGTGA GCACCATTGT TGAGTCCAGG 480 GCCTGGGCTG TGGGAACCCC TGCACATATA CAGGTGCTGG GGCCGCCCAG TGTGGCGATT 540 GAAGCCAAGA TTGGCCCCAG GCGCTGATGC ATCTAGGTTG TTGGTGGCGT GTTCCTCCCG 600 GGCAGGAGAG CTAGGGTCCA GGTTCACGAA GAGTGCCTAG CACTGCCATG CTGGCTTTCT 660 GAGGGCTGCA GGTCACCATG TCCCTCCCTG GGGTGTCTGG GTGGGAGGGG TGGAGAGCAG 720 GACTTAGCCA ACTCCATCAG CTGCTGCTCC TGTGCATCCT GTGGTGGGTG CTGGCCTCTC 780 CGCCCCTGCC CCACTCTCGC GAGAGAGCTC AATCAAGCAG CACCTTCTCC TGGCCTCCTC 840 AGATATGCCA GGTCCCCTCC TAGGAACCGT GAACTAGAGA GACCAGGTTC CTGCCCTCGA 900 GGAGGGGGAC ACAGCCTAGG TGAGCATCTC AGTGCCGCTG GTTGCTGTGA AGCCTGTGAG 960 ACAGGGCTGC GTGTCTGAGG GGTACCCAGA 990
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