| Tag | Content |
|---|
EnhancerAtlas ID | HS101-28225 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr21:37431400-37432570 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr21:37431769-37431784 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TATACTGTGA GCTAAATCAT GATCCCTACA GTAACAGAAT TCCCATTATA TCAGTCCCTC 60
TAAAACAGTT TTATCTTGCA GACCTAGTGA CTACAGCTTA ATCTACTAAA AATACAAAAA 120
ATAGCTAGGC GTGGTGGCAC ACGCCTGTAA TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG 180
AATCGCTTGA ACCTGGGAGG CGGAGGTTGC AGTGAGCCGA GATCGCGCTA CTGCACTCCA 240
GCCTGGGCGA CAGAGCGAGG CTCCGTCTCA AAAAAATAAA AAAATAAATA CATAAATAAA 300
AATAAAATAA TGGCTGGGTA CAGTGGCTCA CGCCTGTAAA ACCAGCACTT TGGGAGCCCG 360
AGGCGGGCTG AGGTCAGGAG TTCAAGACCA GCCTGGCCAA CATGGTGAAA CCCCGTCTCT 420
ACTAAAAATA CAAAAATCAG CCGGGCGTGG TGGCAGGCAC CTGTAATACC AGCTACTGGG 480
GAGGCTGAGG CAGGAGAATC GCTTGATCTC AGGAGGCGGA AGCTGCAGCT AGACGAGATC 540
ACGCCACTGC ACTCCAACCT GGGCGACAGA GCGAGACTCT GTCACAAAAA ATAAATTAAA 600
AAAATAAAAA TAAAAAATAA ATCTACTTCT AAAACATACG AGGGCAGAAA TGAGCAAGAG 660
ACAAGAACTC CAGGCAATAT TAATACCGCA CTTCCGCAGT ATAAGGTTCA TTATTTGACC 720
TAACGAAAGT CGGCATGTCC AGCTCCAGAG GCGAACGGCG GCTGGTTCGG TGCGGGTCCC 780
AGCGCTCAGT CCACAGACCG CGCCGGGAAG TGTCCCCAAG ACTCCCGGGC CCTCGCGCGA 840
GCTGTCCACC ATCACCCTGC TGAGGACCAC GTGAAGCCCG GTGACCGCCA CAGACACAGG 900
CACCGTCCCC GCCCCCATAG TCCTCAAACT CTAGCCGTGA GGCCGTCCTA CGGTCCGACA 960
CACACCGCTC CCGCAGCCAT AGGCCAGCCA GGCGAGCATC GGACCTCGGG CCTCAGGCTC 1020
CTCAGCTTTA CGCAGCGCGC CGGAGCAACA TGCGCTAAGT GTAGGACTCC ACAAGATGAG 1080
AGGTTACTGC AGCGCACACG ATAATGCCTG CCCTGGAGGG GACCTGCGAC CTAAACTCAG 1140
TTCTTTTTAC GCTGATGAAT GAAAGACTAA 1170
|
