| Tag | Content |
|---|
EnhancerAtlas ID | HS148-09893 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr2:132426540-132427680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr2:132426672-132426690 | GGCTTGCTCAGGCATGTC | + | 6.37 | | TP53 | MA0106.3 | chr2:132426672-132426690 | GGCTTGCTCAGGCATGTC | - | 6.5 |
|
| | 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 |
| GH02I131667 | chr2 | 132425552 | 132428164 |
|
Enhancer Sequence | GGGCGGGCTT AGCAAGCTTA CAGAAGCAGA ACAAAGGCAG TTAATCAAAC AGTGACAAGT 60
GTATGACTCA AACATGTCTG ATGACCTCTG CTGGGCCACC CAGCAGGCTC TCAGCAGATG 120
GTAACTATTT TAGGCTTGCT CAGGCATGTC TTGTGACCTT CTCAGGGTCA CACAGATGGA 180
AAACAGGAAC TTAAAAAATC CTTATAAACT TACAGAGATA GTTACAAAAA TAGTTATGAG 240
AGCAGAACAA AGAAATATTG GCCTGGGAAA GAATCTCAAA GGGGGAAGCT GATAAGAACT 300
TGTTTTTCTC ATCCCTGTTC CTGGAGTCCA TTCCTTCTGG GCTCTTCCTG GCCTTGTATA 360
TAAAGTTATC TTAATTCTAG CACGGCCTTG GAGTGAGTCA GCCTGGAACA GGCAGGAACT 420
TAGGTTTTTC TCTTTTTAAT TTCTGCTTTA GTAGGCCAGG GTTCTGATTT TCACTGCTGA 480
GAAAGTAAAG TGTGTTCAGG CTGCCCATGG TTCTGGGCCC CCCCGGGTCT CTGAGGAGGG 540
CTGTCCCCTC CATCACAGAG AATATCAGGA CACTAGCTTG TTCTAGTTAT ACTTACACAC 600
TCCTCTCATG TTGTCTATGG AGTGGTGGAT GCTGCAGGGA GGGTGACATC CTAGTTAGTC 660
CTAAGAGCCA GACTGCCTGA AGCTCACTAT AACAAGTCCT GCCTTGGGGA AGAAGGAAGT 720
GTGTCTCTGT GAACCTCCCA CCTGGGCCGA AGGGAGGCCA CTCTCTCTGC TGCCTCTCCC 780
CAACCTTGGC CTTCTGTGCT CCTAGTGAAC CTCTCACCCC CTGCCTACAG GCCTCGAATC 840
TCAAGACCAT GATGACCTCT GGTCACCCCT GAATCCAGAG CTTTCCTTTT ACAAAGGGGA 900
AACTGAGACC TGGAGCAGGG CTGATGTTCA GCCAGCGCAC AACGGAATGG CCGAATTGGT 960
GGTAAAATAC TGAAATAGTT CCAGTGTGGA TGGAAAGGGG CTGCTGCCCT AAGCATCTCT 1020
ACTGCCCACC TCATCCCTTC CTCCAGGACC CTGGGTCAGC ACCAGGAGCA TCAAAGTGGC 1080
CAGGATTGGC CGGAGCCCAT GCTAATGGCT CTGCCAGCCC TTCTCCCCAC CAGAGAGGGC 1140
|
