| Tag | Content |
|---|
EnhancerAtlas ID | HS091-49147 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chrX:15489070-15490200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:15489310-15489329 | TACCCACTAGATGGCAGTA | + | 6.54 | | JUN(var.2) | MA0489.1 | chrX:15489374-15489388 | ATGAGTCACTTCTT | - | 7.04 |
|
| | 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 |
| GH0XI015471 | chrX | 15489123 | 15489524 |
|
Enhancer Sequence | AACTCTTGGA ATGTAGCCTT TAAGACATGA ATGGTTTTTG TTTGTAATTG CAATGTGGTG 60
TGGGTAGGAT GTATAGGGAA ATTTGTTGGG AATTTATTTG GACTACTTTC AAAGAATATT 120
TCAGTTAAAT TTCTACTCTC CCTCATGTGA CCTACGCTTG TTAACACAGA CGAGGCTTTA 180
ATTCTTTGCT GTGGGAAGTG GCCTGTGCAC TGTAGGAGGT TTGGCAGCAT CCCTGGCCTC 240
TACCCACTAG ATGGCAGTAG CACTCCCCAG TTGTGACACT CAGAAATGAC TACAGAAATT 300
GCAAATGAGT CACTTCTTGG GCTTTTGGCT AAGATCAAAT GTAGAAATTG CCATATGACC 360
CAGATGGACA AATCACCTCC AGTTGAGAAC CACTGACATA GACAGCACTC CACAAAAAGC 420
AGAACTTTTA GGCTAAAGAT GGTTTTATTT TAACGTGATT GTGTTAAGTT GACAGTTTCA 480
GGATGTGAAA TATTGTTCAT TCATCTATAG CTAGAGATCA AGCTTGGGCT TCGAAGCTTG 540
GGCCTTCCCC AATAATGGCC CAACCTAAAA TTTTAGACCC TATAATACTC CTCCACCTCC 600
CATCCTTCCA CATCCCATTT GTAAGCCCGA TTAGATGACT CACTGTTTCT ACTATATCCC 660
CATACCGCGA CTTTCACCTT TACCTCCACT ATCCAGAGAG TCAAATCTTA CTTATTGGTT 720
AAGGCCTTAC TAAATGGGCA AATTTTCCCT GAAGCCCTCC CAGATCCTTC TGTTAGAAGG 780
GATAGCTTCT GCCTCAAAAC ATGAAACTTC TTCAACTATA CCCATCTTGT TCCTCCTTAA 840
TTATTTTCTA ACTTTCATGC AATTTGAAAG TCCTCTGCCT CCACTTCTAA ACTCATGAGT 900
GCACTCACTA TTTTAATATC CTTTCAGCTA GGCAATGTGT TGTGGAGGAG AAAGTTATGC 960
TTTTGATTTA AGGCACTCCT AAATCTCATG CGCCCCTCTA ATGGTGCACA GATGTTTTCT 1020
AGAGAAAGTC CTCATCCCCA TTACACAATG GCATATATTA TTAGCTTATC TGGTTGACAG 1080
GAATAGAACA CAGGTAAGGT TCACTTTATC TGGAGAGGGC AAACCCAAGT 1130
|
