| Tag | Content |
|---|
EnhancerAtlas ID | HS048-31480 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr6:31334420-31335230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:31334840-31334859 | CAGCGCCACCTGGTGGTCG | - | 8.69 | | FOXP1 | MA0481.2 | chr6:31334530-31334542 | TTCTGTTTACCT | - | 6.14 |
|
| | 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 |
| GH06I031366 | chr6 | 31334378 | 31335285 |
|
Enhancer Sequence | GTTGTGGAGG TTCCTTGAGT TCTCTGCTGA GAACTAAATT AATTCTATCC TTTGAAGGTC 60
GATTCTTCCC AGGAATGGAG AACCAGGTCT TCCTACACAA AATCACCAGA TTCTGTTTAC 120
CTTCTACTGA AGAGATTGTG TCATTCTCTG GAAATACCTA AATTCATTCC TGAGCGGCGG 180
TCAGGGCAGG TCCCCGTTCT TGCCGATGCC CATGTTCTGA GACACAGCGA CGATGCAGTT 240
TAGCAAACGA ACCATGACAG CAGCGGTGAG CTCCTCCAAG CCCGCTCGCT ACACCAGGAC 300
GCGCGGCCAA GATTGGCCGG AAGGTTTTTA CTTGGAAACT GGAGGATGAG CCATGACATC 360
CCTCTCTCCA CCTCAAAGCT CGTCCTGGGC ATCCACCTCC AGGGAGCAGA AGCAGCGCAG 420
CAGCGCCACC TGGTGGTCGA TGCGCTTCCT TTGCAGATCA CGCACAGCCC TGAGATCCAC 480
CTCTCCTTCC TACGCACCAC GCATTTCTTC ACTGGACACC AGCCTGCGTC AATCTTCCTG 540
TAAAGCAAAA GAAGCGTGAG GTTGGTGGGG GAGGAATGGT GTTATCTCCA CCTTTGGCGA 600
GATCCATGTC ACCGTGTTCA GGGGAAGGGC CAGGCCTTAC TCCCCATGCA GAGAGGAGGC 660
TCTGGCCGTG AAGGCGCCTG TGGAGAGGTG AGGACCCGCT CCCTCTACAC TGATGGCCAA 720
GAGCCTGCAG ATGGCAGGGA AGGCTTCCCT TCAGCTGTGT CCTATCAGGT TCTTCCAGGA 780
GTCCAGGAGT AGACCTGCAT ATTGCCTCTG 810
|
