| Tag | Content |
|---|
EnhancerAtlas ID | HS184-31047 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr9:91636650-91637770 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPIB | MA0081.2 | chr9:91636668-91636680 | TACTTCCGCATT | - | 6.62 |
| | | 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 |
| GH09I089020 | chr9 | 91635029 | 91638991 |
| Enhancer Sequence | CCTTGAGAGA TGGAGGGCTA CTTCCGCATT GCCTGTTGTT GCCCTCTAAG ACGTTTCTTT 60
TTTAGCCATG GAAAAACTCT GTCACACACA GCCCTACCTG GATACCCAGG ATATATGACT 120
TGGGAATAAA ATGGGAGGAG GTCGGCCCTG GAGCATTCTC AGGACTCTGC CTGCCCCTGG 180
GGGCTTCCAG AGCAAGACTA CGGGGTGGTC TTTCCCACTC AGAACTTGTA AGTCACACGA 240
CTTGCCCGAG CCAGAGGTGA CTGAATGGGC TGCGTAATTT CCATATTTCC TTTGTAGCGA 300
ACAAAGGCAC AATGTCAATG AGAGAAGTCA GCTGGTCCTC CAGCAAACAG AACTGAGGCC 360
TCAGTTCATT TTGCTGAGCA GGGAACTCCG CCCCACCCCA CATCCCAACA GGGCTGGACC 420
ATGATCTTAG CCAAGACCCA GGGCAGGAAC CTGAAGAGCC TCGGGCACTA TTTAAACACT 480
TTGGCGGTCC TGTCGGGGCT CCAGGAGCCT AGAAGGAGAT TCAAGGACAC TTCAGTGCAG 540
GAAGGGAGGG TTGGGGGAGG GGGGAAATTC CTACAGTGGG GAAAGCTCAG ACCTCCCACT 600
TCCTTCTTCA AAGCCTGCTC CACCAGTCTG GCCACCGTCA CCTGTGGCTT TGCGGCGGGA 660
TAGGTAGTCA AGGAAGTTTT TGGGACGTGG CAACCGTGGG ACGTACAGTC AACACAATAA 720
GCCTCAGCAT TCACACTGTA GTCCAGCTAA TTCAAGCACA GCTATCTTCA GTAAGGAATT 780
TCCCCCTCTA GAGAGCATGC GCACTTTAAT TTTAGTTGTC CTCAGAATGA CCCTTTGCTC 840
ATCATAATAG CAAAAAAACA CAACCCTGGG TGGAGATTTA AGATGCTAAT GAGATGTGAC 900
TTATGAACAA GCATGTACAG CTACTGCGCA TGTGCACCCA GAGGACCATC CGAACATGCT 960
TATAGCAACA CCTCCTTATG AAAAATCATG AAAGCCTCCC ATAAAGGGAG TCTCCCCTAG 1020
TGCCCGTCTT TAAAATAAGT GCCTAGTGCA CTTATTTTAA GTGCATCTTA TTTATTTATG 1080
GATTTGTCTC ATCCTTACCC CGAAGCCTGC CCTGAATTCT 1120
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