Tag | Content |
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EnhancerAtlas ID | HS053-19750 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr19:45273470-45274770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr19:45274097-45274116 | GAGCGCCCTCTTGTGGCTA | - | 7.32 | ZNF263 | MA0528.1 | chr19:45274305-45274326 | CCCTCCCTTCTTCCCTCCCCA | - | 6.28 | Zfx | MA0146.2 | chr19:45273552-45273566 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09606 | chr19:45273041-45274338 | CD14 | SE_27905 | chr19:45273138-45274246 | Fetal_Intestine | SE_53360 | chr19:45273468-45274190 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I044769 | chr19 | 45273194 | 45274630 |
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Enhancer Sequence | ATTTCAAAGT AAAAGTCATG GTTTAAGAGT CTGTGATTTT GGCCAGGCGC GGTGGCTCTC 60 GCCTGTAATC CCAGCACTTT GGGAGGCCGA GGCGGGCAGA TCACTTGAAG TCAGGAGTTC 120 GAGACCAGCC TGGCCAACAT GGTGAAACTC CGTCTCTACT AAAAATACAA AAAATTAGCC 180 AGGTGTGGTG AGATGCGCCT GTAATACCAG CTACTCGGGA GCGTGAGGCA CGAGAATCGC 240 TTGAACCCGG GAGGCGGAGG TTGCAGTGAC TAGAGTTCGC GCTACTGCAC TCCAGCCTGG 300 GCGACAGAGC GAGACTCAGT CTCAAAAAAA AAAAAAAAGA AAAGAAAAGT CTATGGTTTA 360 AGGTTCTGTG TTTCCGAGTA TCTCTAAGTC TGTGCATGCA TTTGTGGTCA GAGTCTGGGG 420 AGCTGGGGGC GTGAATGGGC TGCTTCAGAC ACTGCTTTGA GGGTGTGACC AGGACCTGAG 480 GGTGTGGTTA AGGTGTAGGG GTGGGGCTAG GCCCTTGGGG GTGGGACCAC AGTCCCAGAG 540 GCGTGGCCAG GGCCTCGAAG GTATGGCCAT AGTTTGAGGC GTGGCCGAGA AACTCCGTTC 600 CCAAGGGAGG TGGTAACTCT GTGCTCAGAG CGCCCTCTTG TGGCTATCCT CAGGTCTCCA 660 CTTTTTATTC AATAGCTTTA TTTCGTTTTA TTTTTTTCAA CTTTCATTTT AGATTCAGGG 720 AGTACATGTG CAGGCTTGTT ACCTGGGTAT ATTGCATGAT GCTGAGGTTT GGGGTACGAC 780 TGATCCCGTC ACCCAGGTAC TGAGCATAGT ACCCAACAGT TTTTCAACCC TTGCCCCCTC 840 CCTTCTTCCC TCCCCACTTT AGCAGTCCCC AGTTTCTATT GTTGCCATCT TTATGTCCCT 900 GAGTACTCAA CGTTTAGCTC CCACTTACAA GTAAGAATGA GCGGTATTTG GCTTTTTCAT 960 CCAGCCTAAC TGTTTTATTG AGATATAATG TGTATACCAT ACAATTTACC TCTTTAAAGT 1020 GTACAATTCT GGCCGGGCGC AGTGGCTCAT GCCTGTAATC CCACCACTTT GGGAGGCCGA 1080 GGTGGGAGAA TTACTTGAAC TCAGGAGTTC AAGACCAGCC TGGGCAACAC AGAGAGACCT 1140 CGTCTCTATA AAAATAAAAA TAAAATTTTA AAAAGTGTAC AATTCAGTGA CTTTAGTATA 1200 TTCACAAAAT AGTGCAATTA TCACCAGACT TTTTTTTTTT TTTTTTTTTT TGAGATGGAG 1260 TCTAGCTCTG TCGCCCAGGC TGGAGTGCAA TGGTTCAGTC 1300
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