| Tag | Content |
|---|
EnhancerAtlas ID | HS092-38892 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:131003140-131004500 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr9:131003179-131003190 | TGGGTGTGGCC | - | 6.62 | | Myod1 | MA0499.1 | chr9:131003656-131003669 | GGGGACAGCTGCT | - | 7.04 | | REST | MA0138.2 | chr9:131003825-131003846 | GGCCCTCTGCAAGGTGCTGGG | - | 6.02 |
|
| | 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 |
| GH09I128241 | chr9 | 131003768 | 131009442 |
|
Enhancer Sequence | GCAGAGAGGG CTTAGGATGA GCAGAGAGGA GTTCAGGGCT GGGTGTGGCC AAGGGGGAGG 60
ACAAAGACTA CAAGTTAGGG TGGGGAGCAG GTGGCAAGAT CTGCTGGTCA CATCGTGGGA 120
CACAGTGGAC TCAATTCCAA AGACAGTGAC AAGACCCTGT GGGGATCCTC GCCTGATCAG 180
GAAGGGGTGA GAGAGGCAGC TGGTGTTCTC CCCTCAGCTC AACTGCTGCT GGGCTGTGCA 240
GCTTGGGTTC TCAGCGAGGT TCTCAGGGAA CCAGAGAGGC ATAAGGAGGG CTCCAGAAGC 300
AAGCCTGGCC CCAGAGGGCT TTGCCGCCAG CCCCAGGCCT CCTTGGGTCT TCTCTGGATG 360
CTCAGAGAAG AAGCTGGGGA GGTCAGCGTC CAGGAGGGAG CAGAAGCAGC TGCCTCATCC 420
TCTCGATCTG ACCCATGACC AGTACCTGGC CAGTGACCCT ACCCCTGAAG TAGAATCCAC 480
AGGCCCTGGA CCGTGGCCAT GGCTCTGGAC AGTCCTGGGG ACAGCTGCTT CCTGCCATGA 540
AAAGGGACCT TAGCTTGTTA CTCTAGGCAC TTTGTGGCTC AGCCCTTGCC CCTGGGGACC 600
TGGAGCCAAA GACCCTTAGA ACCGTACTAT CATAGCTTTT ATTTATTCAT ACTACAAATA 660
TGTATTGATC ACTTACTATC TGCCAGGCCC TCTGCAAGGT GCTGGGATGT ACTAGTGACC 720
AACAGTTCAT GATTTAGCAG GGGAGGCTGC ATCGACAGAT AATCACACAC ACGCACGTAG 780
AGAAGTTAAT TAAAAATCGA AGCCCTTGTT ACAGAAGTCG ACTTCAGGGA GTGATCAAAG 840
ATCATTATGG GAATCCTGAT TTATACTGGG GGACAGGAAG GGGCTGCCTG AGAATGTGAA 900
TCCTGAGCTG ATACTCAAAG GCTGAGTAGG AATTTGCCAG GCAAAAAGGA AAAAGTGCTT 960
TCTAGGCAGA GGCGGCAGCA GCATGTGTAA AGTCAGAAAC ACATCTCAGA ACAGATGAGA 1020
CCTTAAGCTT CCAAGACTCG CAGTTGGCTT CCCCAATCGG CCCCATAAAC TCTGCTTGCA 1080
TACTTTTAGT GACAGGGAGC TCATCCCCTA CCCAGGCCTC CAGTCCCTTA ACTCGGCCAG 1140
GTCTGCCTGT CAAAGGCTCT TTATCCTGAG CTGATCTCTG CCTTCCTCTG TCTTCCACTC 1200
TGTTCACTTG TGGTTCAAAC CAAGGCAGGT CTGGCCCCCA CCCTCCCTGA CTGCCAGGCC 1260
TCAGAGAGCT GGGAGAGGGG TGGGGTTTCG AATGCCTCTC TTTGCCTACC CCATCCCCCA 1320
TGGGGAGGCT CAGGCCCTGT CCACTGACCT CCTGCCCCAT 1360
|
