| Tag | Content |
|---|
EnhancerAtlas ID | HS092-04893 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:224565340-224566770 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ALX3 | MA0634.1 | chr1:224565766-224565776 | TTTAATTAGA | - | 6.02 | | FOSL1 | MA0477.1 | chr1:224565544-224565555 | AGTGACTCATG | + | 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 |
| GH01I224376 | chr1 | 224564092 | 224568999 |
|
Enhancer Sequence | CTGGCTAATT TTTGTATTTT TAGTAGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCT 60
CAAACTCCTG ACCTCAAACG ATCTGCCTGC CTTGGTCTCC CAAAGTGCTG GGATTATAGG 120
TGTGAGCCAC TGCGCCTGGC CATGTAGATG ACTTTTGACC AAAATGTTTC ACCTTCTCAT 180
TCAGATATTC TTAGTAACCA AAACAGTGAC TCATGCAGTT GAGAGAGCCT TTGGGCTGTC 240
AGTTTACAGT ACATCAGGCT TGCTGAGGCT AAGCAAATCA GAAAGGTGCC ATGTTTATAA 300
CAGAGGTCAA AGCTCCTTAC TTCTGAAACA TTAGCTGTGG TTAAAAACAA AAACTCTTCC 360
TTCTTGTATT GCTTGTCTAT CAAAGCCAGG AAAGTGGGGG ATCACTGTAG TTAAATTTTT 420
TTTTTTTTTA ATTAGAGACA GAGTCTTGCC CTGTCGCCCA AGCTGGAGTG CACTGGCGCA 480
ATCGTGGTAC ACTGCAGCCT TGAACTCCTG GACTCAAGCA GTCCTCCTGC CTCAGCTTCC 540
CAAGTAGTTG GGAGTAGGTG CACACCACCA TGCCCAGCGA ATTTTTTGTA GAGACAGAGG 600
TCTTGCTATG TTGCCTAGGC TGGTATCAAA ATTACTGGCC TCAAGCGATT CTCCTGCCTC 660
GGCCTCCCAG ATGTTGGGAT TACTGGTGTG AGCCACCACG CCCAGCTCAA AAACAATTTT 720
TTTAGGGGCA CTTCTACAAA TCATGAAAGG GGGATAAAAG CACTGACTTT AAAAAGCCAT 780
GTTTAAGATG CTATAAATGT TCTCCCCTTT TCATTGATTG GAGAGTTGTA GAGGACCTTA 840
GAGATCATTT TGTCTAACTC CCTCATCCCA AAGATAAACT GAGGCCTAGA GATCGTTCAG 900
GGTGTTGTAA CTGGGAACAT CTGAATGCTG AGGCCTAGAG ATCGTTCAGG GTGTTGTAAC 960
TGGGAACATC TGAATGCTGA GGCCTAGAGA TCGTTCAGGG TGTTGTAACT GGGAACATCT 1020
GAATGCTGAG GCCTAGAGAT CGTTCAGGGT GTTGTAACTG GGAACATCTG AATGCTGAGG 1080
CCTAGAGATC GTTCAGGGTG TTGTAACTGG GAACATCTGA ATGCTGAGGC CTAGAGATCG 1140
TTCAGGGTGT TGTAACTGGG AACATCTGAA TGCTGAGGCC TAGAGATCGT TCAGGGTGTT 1200
GTAACTGGGA ACATCTGAAT GCTGAGGCCT AGAGATCGTT CAGGGTGTTG TAACTGGGAA 1260
CATCTGAATG CTGAGGCTTA GTCCAGTGTT CTCTCTCCCT TACCACTCCT CTTCCCCTTC 1320
CCTCTATAAT GGCAGTACCC AGGGCCCGGT CCATAGACTA CTATCGAGTG CTCCTATGTG 1380
CATCTTAGTA CGTATCATTT TCCCTTGCCT TTTTCCTTCT ATCCTTTCAG 1430
|
