| Tag | Content |
|---|
EnhancerAtlas ID | HS101-16771 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr16:29776420-29777490 |
Target genes | | Number: 28 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr16:29776982-29776993 | GGCCACACCCT | + | 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 |
| GH16I029765 | chr16 | 29776553 | 29777479 |
|
Enhancer Sequence | TCCGCCTCCT TGGTTCAAGC GATTCTCCTA CCTCAGCCTC CCAAGTAGCT GGAATAACAG 60
GTGTGTGCTA CCACGCCCGG CTAACTTTTG TATTTTTAGT AGAGATGGGG TTTCACCATG 120
TTGGCCAGGC TGGTCTCAAA CTCCTGACCT CAAGTGATCC GCCTGCCTTG GCCTCCTAAA 180
GTGCTGGGAT TACAGGCGTG AGTCATTGCA CCCGGCCTGG ATAATACTAG TTTAGATAAA 240
CCACTTCATA AAGTGGGTAT GCAATGCTTT GTTTCCTCTC ACCTTGACCC AGCATTGCTT 300
GTCATCTCTG AAAGACCACA AAGAGACCTG CCCCTCCACT TCAGGGACCC ACTTGAAACC 360
TGGTCACCAT CCAGGCTTGC TCTGCCTTGG CCATCAGGTT CCCTGGGCAC CAAGCCTCTC 420
TTTTCTCCCG CTGCACCTGC CAGCCCGTCT GACAGCACTG GATCCTGCAC CCTGGAGTCC 480
GTTTGGACTC ACCTGCCCTG ACCTTACTTG GCTTCCTCTG TGATGTTGAC TTTATCGACC 540
GCTTTTGCCA GCCTGGTCTG TCGGCCACAC CCTACCCATA AATCTTCTAC CTTGGATCTA 600
TACAACTGCC TCCCTTTTGT CCTGTCCCCA GGGTAGTGAG CCCTCCAGGG CCTGCAGCCC 660
CAGCTGTCCT GATCCTTTTC TCCTGAAGCA AAGGAAGATG TGTTCATAGT GTACCCACTG 720
CTGATCTTTC TCCTCTGTCC AAACATCTCC AGTCCTGTGC TACTGCCCTG GACATAATCG 780
TTTATTTTGT TTTTTTGTTC TTTTTTTTTT TTTTGACACA GAGTCTCACT CGGTAGCTCA 840
GGCTAGAGTG CAGTGGCATG ATCTTGGCTC ACTGCAACCT CCACTTCCCG GATTCATGTG 900
ATTCTCTTGC CTCAGCCTCC CGAGTAGCTG GAATTACAGG CACGCACCAC CTCACCTGGC 960
TAATTTTTGT ATTTTTAGTA CAGACGGAGT TTCACCATGT TGGCCAGGCT GGTCTCAAAC 1020
TCCTGACCTT TGGTGATCCA CCCACCTTGG CCTCCCAAAG TGCTGGGATT 1070
|
