| Tag | Content |
|---|
EnhancerAtlas ID | HS089-05649 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr17:21098880-21099960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr17:21099081-21099096 | TATTTCTTGAGAAGT | + | 6.31 | | TFAP2A | MA0003.3 | chr17:21099228-21099239 | AGCCTCAGGCA | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCAGACTCCT GAGTAGCTGA GACCACATTT GCGTACCACC ACATCTGGCT AATTTTTGTC 60
TTTTTTTGTA GAGACAGGTC TTGTTATGTT GCCCAGACTG GTCTTCAACT CTTGGACTCA 120
AGTGTTTAAT GGTCCTCCTG CCTCAGCCTC CCAACGTGCT GGGATTACAG GCATGAGCTA 180
CTGCACTCAG CCTTCAAATG CTATTTCTTG AGAAGTACTG TCGCATATCA CAGATGACCA 240
TAAGCAACTT GTCAGCAGCT CTGCCATGAC TGATCATCTA GCAAGGACAA TGGCAGGAAC 300
AGAGAAGTCA GCACTGACAG TGGGAAGGGA GGCACATTTC TTGCTGCCAG CCTCAGGCAC 360
ACGAAACCCC TGCCTGCAGT CCACACCAGC ACCTCATCCC CATCTCCCTG GCCAGGGGCC 420
ATGTAACTAA GATGGCATTT CAGAATCTAG GTTAATACAT CCAATAAGAA TCACTTGGTT 480
CAGTGCAGCT TGGGAAATGG TAGAAGAGCT ACCCATTTGC AGCTGGATTC TACCTCGGGG 540
GAGGGCTCCT GCTCAGCTGA CTTGAGGTTG CCTCGACTTG TCTGGCTTGT CCAGCTTGTG 600
CCTTCTAGTC AATTCCCCCA TGAAATCTAA CTTGTTGGCA GAGCACTTCC AGGCCAGGTA 660
TGGGGCTCCC TTTCCAAACC TGGGCATTAT TAAGAAAAAA AAAAACCAAA AACCTGCCCA 720
GCAGGCTCAG ATGCCAGCAC TCAGACACCT GAGGGGTCAT GGGCAGCTGC ATTTCAACTC 780
ACACTGCTGT CGAGATGAGG CATGTTTTTA CGGGATCAGT TGTGTGGCTA AGGCAGTTCC 840
CTCTTTACCA TTATTCCAGG TGCCCAGAGA CTGCCACGTA AACAGTGGTG CACACCCAAC 900
ACCGTCATGC CCCCAGCACT CAACTGAGTG ATAAGTTATT TCTAAATCTC TTGGAATTAA 960
ATCAAAGTTT CTTAAACTTT TTGTGGGCCG TGGGTCCCTT TTAAAATCCT TAAGAGGTGT 1020
GAATCTCCCC TACAAAAAAT GGCCCAATCA CCCCTCGTGA ATCCTTCCCA TGCACCCTTT 1080
|
