| Tag | Content |
|---|
EnhancerAtlas ID | HS184-11708 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr15:89899820-89900940 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| mix-a | MA0621.1 | chr15:89900648-89900659 | AATTAATTAGT | + | 6.62 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTGAGGCAAA TTGCTTAACC TCTCTGTGCC TGGGTTTTCC CATCTGCCGG GTGAGGATAG 60
TAAGAGCAGC TCTGGCATAA GCACAGCTGT GAAGATTAAT AACAAAGTGC TTGGAGTCGT 120
GTTTGGCACA GCATACCCAC TCGGTAATCG TTAACTGTTA GCAAATTCTC ACCCTGTGAA 180
CAAATCTGAA AAATGCAAAT CCTAAAACAT TTTAAACGTT AATCAATAAA CTCATCATTC 240
TGAGCTGGCG TCCAAATGGA TTGCAAACTG TGTTTGTCAC AATTGCCACG TGGTGGCGTG 300
CCTGCTGCTG GCTCTGGGGA AATTGAATTA TGCCAGTTCT GAATGGTGCC AGCCCTTCAG 360
GAGGCTGGCC ACCATGAGAC GTGCTAGATG TCCTGCAGTA CAGCCCAGGG GCTGCTTAGG 420
CGGGAAGGCA CACAGAGAAA AAGGGCCGGG CTTGGCAGAA GGGGGTTGGG GTCAGAGGGC 480
TGGCAGGAGC AGAGGACAGA ATCCTATGCA AAGCAGGCCA GAGGAAAGGA GTAAGACTCC 540
TGCTAGGGCA GGGCATAAGC CATCTGAGAA AGTCTCTCTC TTGCCCTTTA TCTCTTGCCA 600
GTCCCATGGC CTTTTCTCCG CTAGTTTATT GACTCGCCTG CTCCATTTTC CCAGTTTCTT 660
TGTCCCCTTA TCACCTGACC ACAGCACTGA CTCCAGAGGC TGTTGAGCTC CCCCTGCTCA 720
CTGCACACCT TCCCAGTCCA GGTCTCACTT CAGTGCTCAG GAGAGACCCT GGTACATTCA 780
GGCCAGACCA GGGATTAGCC CTCGGGGGTC AGTGGCCATG CCAGCTTCAA TTAATTAGTT 840
GTCAGCGGGG AAGGGAGGAT GAAGGACATA GAAGTATGGC CAGTTAGGCC CATCCAGTCT 900
TTAGGTGAAG GAAGAGGCCA CGATGGATAT GTTCAGGTCA GAAAGTTTCA TGGAGGAGTG 960
ACATTCACCG AGAATCTGAA AGACACCCCA GAGGGAGGAG TATTCCAGGC AGAGACACTG 1020
TAGGGTCACA CAAAGGCAGG GAGGGGTGCA AGAGCTTGGG CCTTAAGGAA ATGAGAGATG 1080
CCTGGGATGG TTGGAGTGTC GGGTTCCTGA AAATGGGAAC 1120
|
| |
|
|
|
