Tag | Content |
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EnhancerAtlas ID | HS098-29235 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:26220450-26221050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:26220971-26220992 | CTTTTCTTTCTTTTTCTTTCT | + | 6.3 | IRF1 | MA0050.2 | chr2:26220994-26221015 | TCTTTCTTTCTTTTTCTTTTT | + | 6.87 | IRF1 | MA0050.2 | chr2:26220975-26220996 | TCTTTCTTTTTCTTTCTTTTC | + | 6 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_26712 | chr2:26220231-26221007 | Esophagus | SE_28420 | chr2:26220324-26221531 | Fetal_Intestine | SE_29154 | chr2:26220039-26221556 | Fetal_Intestine_Large | SE_32014 | chr2:26220291-26221047 | Gastric | SE_35193 | chr2:26220282-26221276 | HeLa | SE_36382 | chr2:26220312-26221288 | HMEC | SE_57610 | chr2:26220451-26220707 | VACO_503 |
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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 |
GH02I025997 | chr2 | 26220270 | 26221869 |
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Enhancer Sequence | GATTACAGGC ATGAGCCACC GCGCCCAGCC AAACTTTGCT CTTTCTTAAA TCTCAGAGTG 60 GGACTGCCAG TGCCAGCCTG GCATTCCCTC TTGAAATCAT CACCTATTTC AGAGGAGGCT 120 GCTACAGTGG GAAGTCAGGA CAACAAGGTT GGGGCCAAAC TCTGGTCTCC CAGGCATTTC 180 ACCTTAATAG GAAAAGTGCC TGAATCTGTC CTCCTCATTT GGCTCATGTG CAGAACAAGG 240 CACAAAGCCC TGCGTCTCCC GGCTGCCTGT CCGATGCCCT TTTCCCTGAC TCACCGTCAA 300 TCAGCAGTCA GACCAAGGTC CCTGACTCAC CGTCAATCAG CAGTCAGACC AAGGTCCAGG 360 CTCTTGCCTC CTGAAATGTT GCAAGGGCGG TTTCCCAGTG TGATTCACAA ACAGCAAGAA 420 TGTTTCAGGC TGACTTGGAG ACCACTTGGG GGTGGTATCC TCAGCCAGGA AGCTTCCTCA 480 GGGCCTCTGA GTCCCAGAGA GCTCTATTTG TCTCTTTCTT TCTTTTCTTT CTTTTTCTTT 540 CTTTTCTTTC TTTCTTTTTC TTTTTCTTTC TTTCTTTCTT TCTTTCTTTC TTTTCTTTCT 600
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