Tag | Content |
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EnhancerAtlas ID | HS118-01690 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr1:214612500-214613550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr1:214613087-214613099 | TACTGTTTACTT | - | 6.18 | TP53 | MA0106.3 | chr1:214612970-214612988 | AACATGTTGCAACATGTC | - | 6.09 | TP53 | MA0106.3 | chr1:214612970-214612988 | AACATGTTGCAACATGTC | + | 6.14 | TP63 | MA0525.2 | chr1:214612970-214612988 | AACATGTTGCAACATGTC | - | 8.48 | TP63 | MA0525.2 | chr1:214612970-214612988 | AACATGTTGCAACATGTC | + | 9.47 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_02460 | chr1:214612564-214613605 | Astrocytes | SE_35815 | chr1:214611152-214622467 | HMEC | SE_45575 | chr1:214610539-214623348 | Osteoblasts | SE_47135 | chr1:214610849-214616152 | Panc1 | SE_56089 | chr1:214610839-214614874 | u87 | SE_58044 | chr1:214613204-214613604 | VACO_9m | SE_64230 | chr1:214611830-214615909 | NHEK |
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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 |
GH01I214437 | chr1 | 214610984 | 214615899 |
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Enhancer Sequence | TTTGCTGATT CCAACAATCA TTCAAAACAT ACAGAGCTCT AGCAGATACA TAACTTGCTT 60 CAAATTTTCC ATCAGTATCC TCATCAGTAG CTATCTTTTC ACAGTTGGCC ATTTTATTTC 120 AAGGATCCAA ATTACCGACC TTTTTCATGT TTTCCTTAGT TAGACCTATG GGTTTCTCAC 180 ATTAGTCACT GTCATAAACA TCTATCTTTT CTACCTTCTT CAAAACATTT ATGCTGGTCA 240 AAAGCATTTG CTTCCAACAT TGCTTCATCT CTGTGATTTT CTACTAAAGG ACCATGTGTC 300 TAACTCGCAT TTCAGTTAAA CTTACGTCAA AGTTGCTGGG ATTTGCTCTG AATAACGGTA 360 ACTCATTTTT ATGCTGGCAG CAAACGTCAG GCGAAATGTC TACTCACTCT CCCCAGCTGC 420 AAGCACAAGA TTGACGAGCT GACCTTGAGA GTTAGGAGGC TGTAAACCGA AACATGTTGC 480 AACATGTCCC GCTATGATTA CGCCTCCTCT GCTTTTACAA AGTACACCAG AAAGCAGTAT 540 CATTATTTGA GTCACACCTG GTAACTTGAC ACCTGCTGAC ACCTTTCTAC TGTTTACTTG 600 CAATGTCTCA ATTTTCCACC CTTCTAAAGG ACTCAGTGTC ATCTGAAAGC TTGGCACTTT 660 CACTATGTGC CCAGGGCTGG AGATCACTGA TAAAGACGTT AAATAAAACC CATTTTAGTT 720 CCACTCTCTA CATAATGCTC GCTATTTAAA GGACTCACTC AAAGAAGTGC CTGTTTCCCT 780 CTACCCTTTG TTTCTTCTGT CTGAACTACT TCCTTCTCTT TGACAAAACT CATCCCTTCC 840 AATTCCACAG TGTGTCTTAG CTGTTACAGC TAAGGGGAGG GGAGGGGAGG ATTGGCAAAG 900 ACTTTTTGAA CGTTTAAATA AATCCTATCT ATGGGCTCTC CCATGTCAGC ATGCTTGGTT 960 CACCTAAAAC CATTCCAGAA CCACCTTAAG AGCCAGGCTT GTCACTAAAC AGCTGTGTGA 1020 CTATGGGCAG AGTCCCTTTA TCTGTCTGTT 1050
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