Tag | Content |
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EnhancerAtlas ID | HS053-11083 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr13:41976260-41977720 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arid3b | MA0601.1 | chr13:41976482-41976493 | ATATTAATTAA | + | 6.62 | Gabpa | MA0062.2 | chr13:41977201-41977212 | GTCACTTCCGG | - | 6.14 | TP63 | MA0525.2 | chr13:41976835-41976853 | GACGTGTCCTGACTTGCC | - | 6.87 |
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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 |
GH13I041402 | chr13 | 41976864 | 41977662 |
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Enhancer Sequence | GAAATTAGAA ATTTAAATTT TTTCAGTGGC CATAAGACTC TAAGCATGTT AAAAACAAGT 60 TAAATATACT ACATATTTTC ATAAATATTC AACGTAAAAG TAAAATTTTA TTGGCCTTTT 120 AAACTTTTAG TTCATGTATC CAATGATTAA ATATTACATA CTGATGACTA TCACTTATTC 180 CTATTATCCC TATTTTTACA GAGATATAGC TGTAATCAAT ACATATTAAT TAACTTAATT 240 CCAATAAATA TGCAAAAAAG GTAACTACAT GAGATGATGA CTATGTTAAT TTACTTGACT 300 GTGGTAACCA CTTCATTATA TTAAAACATC CCATGTTGTC AACCTTAAAT ATCTGCAGTA 360 AAACAATTTT TAAGTATATA TTAAAAATCA ATCAATAAAA AGGCAGAGAA GATTAGAAGT 420 AATTTGTATA TCAATATCAT TCAATAATTT AAAACTTTTC TCAATTTTAT GCCAAAAATT 480 ATGGAGTGAT GTCCATCAAA CGCCTTTTAT TAAAAAGTCT ATCTGTGGAC AACTTGAGTA 540 GCGCCTTCTT CAATTTTGAC AGAAGCAATG AAGTGGACGT GTCCTGACTT GCCTGGTAGC 600 CGAGGCTTCA GTGTCCCACC CACCTCCTAT CGGCAGTGCT CATATCAGGA CATGCTGTTG 660 GGTGTCTGAC TGTAAATACA CATGTCTGTC CCCGGGAGAG CTTCCCCTTT GCCTGAGTGT 720 GAGGGAGACG AGGGGCAGGG AGGTAATGCC CTGGGACCAG CCCTAGGTGG ATGACAAAGG 780 AGATCTGGAG AATAAACACC CCAGCTTCCC AGCCTGTCAG GTGGGATAGC CTTGAGTGCT 840 CCACAGCAGC TCCCAGAGTC TCCTACCTGA GCTCAGGCCC AGCCTCTCAC AGTGGTAATG 900 TGCTCAGTAA GGCACTCTGT ACCAGCTTCC TTCTCTTCAC AGTCACTTCC GGCTCCCCTC 960 TGGTGCCTCC TGGGATTGTC ACAGGATCCT TAGGATGTCG CTTCACCAGC CGGAAACCTC 1020 TGTGGCCAGT GGCACCTCTG CTTGAGTTTT GCTTGCACCC ACTGGGTTTG TTCTGCCGAC 1080 TCGGCCCGTC AGGCTGCACT TGGCTTGTGC TACCAGCCTG GATCCCACTC CTGCCAAAGT 1140 CAAGCCAGGC ACAGAGAGGC AGGGAGTGTG TGAATGAGCA ATCACAGGGT CTGGCCACTG 1200 TGCACAGCCA GGTGTGCCAG CTGCAGCAGG GTGGGCAGCT CCAGGCACTG GCACAGGCAG 1260 TGCCTTTGTG CGAGGCTACG GCTGGACCAG ACATACTACA AGCGGCTTCT GCTTGTATCC 1320 AGACTAGTGT CTGGGCAAGG TGGAAAGCAG TGGTGCCTGA AAGCTTGCAG AGCCCCAAAG 1380 AGAGTGTTAT AGCACGTCAC AGCCCTTGCT TGGGAGCCCC AAGTTCTGGG CTCCTTCCAC 1440 CTCTGCCCAC CTGACATAGT 1460
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