| Tag | Content |
|---|
EnhancerAtlas ID | HS098-11978 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:132271700-132272750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2A | MA0003.3 | chr11:132271870-132271881 | TGCCTGAGGCT | - | 6.32 |
|
| | 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 |
| GH11I132402 | chr11 | 132272081 | 132272230 |
|
Enhancer Sequence | TCTTGTGACT CCACATTCAG CATGCTTTCC CCACACCAGG CTTACTGAAT ATCCCTCCAA 60
GGACGCTGCT GTCTATCAGA ACTAGCAGGA AAAAACATGG TCTTTGCACA ATGGGAACTT 120
AAGATAAAGA AAAGAAAGAG AAATACCTAG GGATGCTTTA AAAAGCAACA TGCCTGAGGC 180
TAACAGGTAA ATGGCCAACT GACCAAGGCA CTGGGGAGCC AAGGGGATTT GGAGTGATCC 240
CAAGTAAGTG GGGTTAATCA GAGGAGGCCA CGTTTCCTGC AGGAGGTGGC ATCGGAGTCA 300
GCCTAGCCAG CAGGTCTGCA TTGCAGAACT CACTCACTGA AGAGCGTGCT ATGCTCACTT 360
GAAAGTGGGT GTAATTAAGT TCTTCCCTGA GCAGCTGCAG AGCATGCAGG TTGCTGGGGC 420
TGCCACGAGT GTATTGCTAG TGCCCCCCTG TGCACAAAGG AAGAACTGAG CAATGTGCGG 480
GGTAAGCGGG GTGGGGATGG AACAGCTGTC TGTGCCCTTC ACCAGGAGCA TGCATTTCCA 540
TTCTCACATC CCTGAAACTG CTCCTTTAGT CTGAGGAGCA TGTAAGTAAG CAGGGAGACC 600
TTCCCCTCCT CACATCCCAG CTGCAGTGAG CGAGTCTCTG TCCCTGGGCA CTCTGTCTGG 660
GAGCTCTGCC ACAGGTACTC GCCTCCACAG ATGTGCTGTG GACAGGGCAA GCTGGAGCTT 720
CCCTTTAGGG AAGGAGCAGG AATTTCACTC CCTGGCCAGG CTCTGTGCAA TTAGGACAGC 780
CTGGTCTAGT TGAAAGAGCC CTGGGCTGGG AACTAGACAC CATGAGCTCT AGATGTCAAT 840
GTTTTTGCCT AGTTTTGTTT TGCTGGGCAA TTTGTTCTCT GGATTTCAGT TTCTTTGTCT 900
GGAAAACAAG TACTGGTTCA CGTGCCGTTG GCCAGTGCGT CAATAGTCCA GTGCCCACGT 960
GGTCCTTCCT CAGCTTTCCA GTACGGTGGT ATATTTGCTC ACCTCCTCTC CTGCCTTGCT 1020
CCTCATTCTC TCTATCCCCT TGGAATTAGT 1050
|
