Tag | Content |
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EnhancerAtlas ID | HS145-22212 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr6:32361470-32362410 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP53 | MA0106.3 | chr6:32362034-32362052 | CACATGCACAGACAAGTT | + | 6.06 |
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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 |
GH06I032393 | chr6 | 32360865 | 32362538 |
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Enhancer Sequence | AACCAGATCA CTGGGGAATG GGCAGCAGGA AATCAAATCA TTATCTTTTA ATCATTTTGC 60 TTCTATTACA AGTGGAAACA CTGACCTCAT GCATCACTGA GCCTGGATTG CATGATAAGC 120 CCTGGGCTTT CCTGTTTCTC ATGTTTCCTT AGTTACTGGA TATTCACTGA CTGCCTCCCA 180 TAGGTGACTT GTGAAAAGGG AGGCTCGGGG AAGTACGCAG TACGGTTCCC ACTGCAGTGT 240 GCTCCGCTGT TTCTGTTTCC CTGACTTACC TCTTTTCAGC TCCTCTTCCT GGGCAGGCCT 300 ACAGCCACAG CAAGAAGCAA TCCCCAAACA AGCAGTGTTT TCCACAAAAA CGTCATCCTG 360 GACTCTAAAA TGGAAACCCA AGAATCCCTT GAAACTGTGA AACTGGGACA ATATTAAGAT 420 TGTACTTTTC ATCTGAGCAG CTTCTAGGCT GGAGAGAAGG GAGAGAATTT GGCCTCCCAG 480 GAAGCAGTTG GCCTGCTCCT CCCTGCTCTG GAGATGCAGA GGAGAGAATG CAAGTATTTC 540 ATGTTTGCTC GTCTCAGAAA TGTACACATG CACAGACAAG TTTTCCCTTC TCTCTTCCAA 600 CTATATCACA CAATCACTGG AATGACTTGA GGAGGAAAGG ATAAAATTAC TCAAGCCGCA 660 ACCATGAAGA TGGTATTAAT AAAAATCAGT TTCTAATCCA GAAGAAAATC CTCCATGAGG 720 GGGAAAACAC AAAGTTCTGT AATTTAATTG TTTTCACATC AGAAGAAGAG AATTTAAAGA 780 GAGAGAGTGA AAACAGGGTC AATTACGAGA ATTTAGTGTG TATCCAATGA TAAAAATAAT 840 TGCAGGGCGC TAGTTGAGGG TGTCAGAGAG AAACTCAGAG GAGTAGAATC CCTGGGTGTC 900 CTGAAAACCA GCTTTGCAGA GGATAGCAGG AGACCTCGTC 940
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