| Tag | Content |
|---|
EnhancerAtlas ID | HS014-00336 |
Organism | Homo sapiens |
Tissue/cell | CCRF-CEM |
Coordinate | chr1:224565360-224566770 |
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 | TAGTAGAGAT GGGGTTTCAC CATGTTGGCC AGGCTGGTCT CAAACTCCTG ACCTCAAACG 60
ATCTGCCTGC CTTGGTCTCC CAAAGTGCTG GGATTATAGG TGTGAGCCAC TGCGCCTGGC 120
CATGTAGATG ACTTTTGACC AAAATGTTTC ACCTTCTCAT TCAGATATTC TTAGTAACCA 180
AAACAGTGAC TCATGCAGTT GAGAGAGCCT TTGGGCTGTC AGTTTACAGT ACATCAGGCT 240
TGCTGAGGCT AAGCAAATCA GAAAGGTGCC ATGTTTATAA CAGAGGTCAA AGCTCCTTAC 300
TTCTGAAACA TTAGCTGTGG TTAAAAACAA AAACTCTTCC TTCTTGTATT GCTTGTCTAT 360
CAAAGCCAGG AAAGTGGGGG ATCACTGTAG TTAAATTTTT TTTTTTTTTA ATTAGAGACA 420
GAGTCTTGCC CTGTCGCCCA AGCTGGAGTG CACTGGCGCA ATCGTGGTAC ACTGCAGCCT 480
TGAACTCCTG GACTCAAGCA GTCCTCCTGC CTCAGCTTCC CAAGTAGTTG GGAGTAGGTG 540
CACACCACCA TGCCCAGCGA ATTTTTTGTA GAGACAGAGG TCTTGCTATG TTGCCTAGGC 600
TGGTATCAAA ATTACTGGCC TCAAGCGATT CTCCTGCCTC GGCCTCCCAG ATGTTGGGAT 660
TACTGGTGTG AGCCACCACG CCCAGCTCAA AAACAATTTT TTTAGGGGCA CTTCTACAAA 720
TCATGAAAGG GGGATAAAAG CACTGACTTT AAAAAGCCAT GTTTAAGATG CTATAAATGT 780
TCTCCCCTTT TCATTGATTG GAGAGTTGTA GAGGACCTTA GAGATCATTT TGTCTAACTC 840
CCTCATCCCA AAGATAAACT GAGGCCTAGA GATCGTTCAG GGTGTTGTAA CTGGGAACAT 900
CTGAATGCTG AGGCCTAGAG ATCGTTCAGG GTGTTGTAAC TGGGAACATC TGAATGCTGA 960
GGCCTAGAGA TCGTTCAGGG TGTTGTAACT GGGAACATCT GAATGCTGAG GCCTAGAGAT 1020
CGTTCAGGGT GTTGTAACTG GGAACATCTG AATGCTGAGG CCTAGAGATC GTTCAGGGTG 1080
TTGTAACTGG GAACATCTGA ATGCTGAGGC CTAGAGATCG TTCAGGGTGT TGTAACTGGG 1140
AACATCTGAA TGCTGAGGCC TAGAGATCGT TCAGGGTGTT GTAACTGGGA ACATCTGAAT 1200
GCTGAGGCCT AGAGATCGTT CAGGGTGTTG TAACTGGGAA CATCTGAATG CTGAGGCTTA 1260
GTCCAGTGTT CTCTCTCCCT TACCACTCCT CTTCCCCTTC CCTCTATAAT GGCAGTACCC 1320
AGGGCCCGGT CCATAGACTA CTATCGAGTG CTCCTATGTG CATCTTAGTA CGTATCATTT 1380
TCCCTTGCCT TTTTCCTTCT ATCCTTTCAG 1410
|
