Tag | Content |
---|
EnhancerAtlas ID | HS098-16338 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr13:96192860-96193820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MYCN | MA0104.4 | chr13:96193264-96193276 | GGCCACGTGGCC | + | 7.22 | MYCN | MA0104.4 | chr13:96193264-96193276 | GGCCACGTGGCC | - | 7.22 |
|
| 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 |
GH13I095540 | chr13 | 96192765 | 96193893 |
|
Enhancer Sequence | AAATATCAGA CAAATAACTA AACAAAATTG CATGCTAGTT AGTGGCTCGG ACTGGGAAAT 60 GAGAAGTGAT GTTAATTCTT AACGTTGGCT ACTTTTGTCA CCTGTAAAAT ATGATCAAGC 120 CTGTTAGTCT AACTTAATAG CTTGAGTAAT TGATATAGGG AGTGAAGTTT TTTTGGGGGT 180 TGGGGAGAGA CATTGCTTTT TTCCACTGAC ACTGACGATA CCAGTTTACT ACTATGTGAC 240 ACTTTTTGCT TGAACTAGAA GAGATAAGTA GTATTTTTCA AGTTTTGAGG TTTGGGTGTT 300 CTGCTCTTGT GGACGTGTCA TGTTTAATAA AGCTTGTTCA CAACTACTGG CTTAGGAAGT 360 GGCTTGCAGT TGACAAGTAT GTGACTTGGA ACACTGGGTG GAATGGCCAC GTGGCCCAGT 420 GGCCCAGGGC CCACACTGAG AATGCAGCAG CTGTGCATGC TAAATCTGGC TCTGTCATTA 480 ACCTGCCGAG GGACCTTCTA CAAATGCTTA ATTCCAACCA TGAAAGCAAA CATAGGCACC 540 GATGCTTGAG AATAGTTGTA AAGGAAATCA GGCCTTGTGC AGAAAATAAA CGGAACTCGT 600 CTGCCTTTCC TTTCTAACAC TTGTTGGAGG CAGGGAGGAA TTCAGAATGA CCAGGCTGCA 660 AGTTACTGTT CTTTGCTTCT AATTAAGAGG CAACTATACG CAAGTGAGCA TAATTAGGAG 720 AAACTGGGGC AGCTGGGGCA AGTATGGGCA AAACTTAAGC CAACTTTGAA AACTAAAGGG 780 CAAATCTCTG GAGTAGTGAG AAAGAGATTT CTCCCTGGTT CCCTCTCTTG CTAGCTGCAT 840 ATGTGTACAA TGACCCCATC ACACTCTGCG TCTGAGCCTC CCTCTCTTTC TAGTTTTTTT 900 CTGTTTCCCC TGTTCCTTCT TGTTTTTCCT TTGTTTGCAC TGTCTGAAGG GGAGGAGGAG 960
|