| Tag | Content |
|---|
EnhancerAtlas ID | HS089-05508 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr17:4948290-4949650 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr17:4948915-4948927 | TACTGTTTACTT | - | 6.18 | | NR2C2 | MA0504.1 | chr17:4948313-4948328 | TGACCTCTCACCTTC | - | 6.35 | | Nr2f6(var.2) | MA0728.1 | chr17:4949281-4949296 | CGAACTCTTGACCTC | - | 6.24 | | RUNX1 | MA0002.2 | chr17:4949047-4949058 | GTTTGTGGTTT | + | 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 |
| GH17I005044 | chr17 | 4947381 | 4949715 |
|
Enhancer Sequence | CTTGGTTCAT GCTCTGTTCC ACCTGACCTC TCACCTTCAA TTCACTTTAG TCCGTGATGA 60
GAACCCTTGG GTCAAATGGG CCTCCCCAAG ATGTCACATC TTTTTCTGAG CGTAAGGTGA 120
CTTATGTCCT TCCCCAAGCA TCTCCTGGCC AATAAACTGC CCTTCCTTAA GATCCAGCTC 180
AGCTTCTACC TCCTGAGTGA AACCTCTTCA TCTTCCTCAC CAGGTGTAGG CTGAGGGCTT 240
CTCTTCCCTC CTCTGAACTC CCATAGAAAA AATTTACTGG CTGGGCATGG TGGCTCACAC 300
CTGTAATCCC AGCACTTTGG GAGGCTGAGG TGGGTGGATC ACCTGAGTTC AGGAGTTTGA 360
GACCAGTATG GCCAACATGG CGAACCCTGT CTCTACTAAA AAAAAATACA AAAATTAGCC 420
GGGCATGGTG GCGTGCGCCT GTAATCTCAG CTACTCAAGA GGCTGAGGCA GGAGAATCTT 480
TTGAACCTGG AAGGCGGAGG TTGCCGTGAG CCGAGGTAGT GCCTCTACAC TCCTGCCTGG 540
GTGACAGAGC AAGATGCCGT CTCAAAAAAA AAAGAAAAGA AAAAATTTAT GTTCCCTTCT 600
TAGGAAGCTG AATCTTGTCC TGCTTTACTG TTTACTTATG TGCTTATCTT GTTTTCCCCT 660
AGTAATTTAC CCCCATTACA TTTTCCCCTC TCAAGAGCAA AGGCCGTATT GGTTTATGTA 720
GCTTCCTTAT TACCTAATTT ATGGTAGATG TTCAAATGTT TGTGGTTTTT TGTTTGTTTT 780
TTTTTTTTAG ACTTTGAATC TCACTCTATC GCCCAGGCTG GAGTGCAGTG GCATGCTCCT 840
GGCTCACCAC AACCTCTGCC TCCTGGGTTC AAGCAATTCT CGTGCCTCAG CCTCCCAAGT 900
AGCTGGGATT ACAGGCATGA GCCACCATGC CTGGCTAATT TTTGTATTTT TTTAGTAGAG 960
AAGGGGTTTC ACCATGTTGC CAGGCTGGTC TCGAACTCTT GACCTCAAGT GATCCGCCCA 1020
CCTCGGCCTC CCAAAGTGCT GGGATTACAG GTGTGAGCCA CCGCGCCCGG CTCAAATATT 1080
TGTTGACCAA AAGAATGGCT CCCTCTTATC AGTAAACTGC AGTGGCCAAA GGCATGGAAT 1140
CTGAGACACC CGCTAGCTGT GTGACTTTGG GAAGTCACTT AAGCTTTCTG TGCTGAAATG 1200
TCCCCAACAG TAATAGGGAC ATAATGATGC CAACTTCATG AGGTTGTGCT GAGGCATCGA 1260
TGGGCACCTG GCCCCATGCC TGGCACATGG TAAGCACTGT CAGTGTTAGC TCCTAGGCCC 1320
TTCCTCCTTC AAAATGTGTC AGAGCTGGCA GCTCACACCT 1360
|
