Tag | Content |
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EnhancerAtlas ID | HS146-09255 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr20:33916860-33917760 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr20:33917525-33917544 | TACTGCCCTCTGGTGGTAC | - | 6.92 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_28226 | chr20:33912499-33917609 | Fetal_Intestine | SE_29043 | chr20:33912331-33917824 | Fetal_Intestine_Large | SE_44275 | chr20:33916175-33917707 | NHDF-Ad | SE_55706 | chr20:33914577-33918491 | u87 | SE_63567 | chr20:33916856-33917680 | HSMM |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr20 | 33916979 | 33917000 | chr20 | 33917000 | 33917200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH20I035324 | chr20 | 33912771 | 33918035 |
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Enhancer Sequence | AATGCTACTG GATCTAGAGG AAATACATTC AATATTGCCT TCATCAAATG TATTCAGCAC 60 TACCCAGGCA TCAAGCACTG TTTTAGGAGC TGAGGCTACA GCAGTAAACA AGAGACAATT 120 CCCGAACTCC GGGAGTTTAG GATGATTAGT CAGGCTGCTG AATGATTTGC AGAATGAATC 180 TGAGATGAAG AGAGTCAAGA GGCAGGAGGA CCAGTGAAGA AGCAGCCGAC AGTGAGTTTA 240 GGTGAGAGGT CAGGACTGGA TCTGAGCATC AGTAGGACAG TTGAGGCCCT GATAGTGGTT 300 GTTTTAAAGA AGGGCTCCTT ATAGTTCCTC CTGCTCCTTT GAGAACCAGG CACGTCACAT 360 TGATGGCAAG GATCACTGAC ATTCAGAAAG ACCAGCTAAA GAGAGGACAA TGAACATGGA 420 AAAACAAGTC CCTCCACTCT AGCTGGGCCC CTTCAGCTCC AACCAACCCC ACAGGGCCAT 480 TCACTCAGCA TTTTGGGGGA AACAAAGTGA GAAAAGAGTG TTACAGCTGC CTCATCAATG 540 GATCCAGAAA TACTCATGGC ACACCCAGGG CAGCTGAAAG AAACATCTGT CTCTACTGTA 600 TCCTAGGTCT GACCTCAGAG CCTCCAGAAC TTTTTTACAT AGCCCCACCC AGATCCTGGC 660 GGAGCTACTG CCCTCTGGTG GTACCCAATG CAGGGGTTAA GCCCACAGGA GAAAAGAGTC 720 TTGTGGTAGG ACATGGAGTG AGAGGCATAG TCAACCCCAA GAGCTCGTCA CAGTGCCTGT 780 ATGTCTTACT ACTGCAACCA CTGCTTTTTC CAAAGACGCT ATTTACAGAA AACTCTGGTT 840 AAAATGCAAG AGTTATCTGG GACCATTAAA ACAGATCCTG TTGGCAACCC TTAACGATTT 900
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