| Tag | Content |
|---|
EnhancerAtlas ID | HS047-35852 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chrX:152126540-152127710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chrX:152127312-152127328 | TTGCTTTCCAGGAATA | + | 7.3 | | BCL6B | MA0731.1 | chrX:152127313-152127330 | TGCTTTCCAGGAATAGC | + | 6.43 | | CTCF | MA0139.1 | chrX:152127603-152127622 | CTGCCGCCAGATGGCGCTC | + | 6.38 | | EWSR1-FLI1 | MA0149.1 | chrX:152126765-152126783 | GTAAGAAAGGAAGGAAAA | + | 6.41 | | Zfx | MA0146.2 | chrX:152127059-152127073 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | 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 |
| GH0XI152957 | chrX | 152126477 | 152128070 |
|
Enhancer Sequence | TGGCTCTCTG CACCATTGCC CCGGGAGCCA AGCCACAACA CAAAAGAATT TTTTTTTAAA 60
ATGCACTTCA GTGTGTTGTT GTTCATTTGG AATGTTCCAC TGTAAGTTAT CTTTCGTAAG 120
ATGTCACCAT TTCTGTAAGA ATTTGCTGCC TCCCGGGCGT AATGTGTAAC CCAGAAGGAA 180
CTCAGTTTTC CAGAAGCAAT TAATAGGTTC CATGGAATGT TGATGGTAAG AAAGGAAGGA 240
AAAGGTGACA AGAGTGAGCG TAGACAGCTC TTTCTAAGGA GTTTGGCTGC TGGAAGGGGA 300
AGAGAAGCAG CTGGGGTTAG GTGGGAGGAA CTAAGTTTAG AGACGCTAAA AGTGTATGTA 360
GCAGGAGTCA CCTGATCAGG TTGAACTGCA GCAGGAACAA GGAAGTTCCA TTTTGACTAC 420
TATTAGTTGC AAATTGGACC CTTATGTCAA CTTTTTCATC TGTAAAAAAA AAGGGATGGC 480
CAGGCACGGT GGCTCACGCC TGTAATCCCA GCAGTTTGAG AGGCCGAGGC GGGCGGATTG 540
CCTGAGTTCA GGAGTTCACA ACCAGCCTGG CCAACAAGGT GAAGCCCCGT CTCTACTAAA 600
ATACAAAGAA TTAGCCACGC GTGGCAGCGG GCGCCTGTAG TCCCAGAATC TCTGGAACCC 660
GGGAGGCGGA GGTTGCAGTG AGTCGAGATC ACACCACTGC ACTCCAGCCT GGGCGACAGA 720
CCGAAACTCC GTCTCAAAAA AAAAAAAAGG GGGGCAGGGG ATGAAAATGC TATTGCTTTC 780
CAGGAATAGC TATGACTACT TCCAATAAAG AAGACAAGAA GGTTCCACAT GTGAAAACTA 840
CGCGGTCACA ACGATAAGTG GGCGGGTGCA CGCACGCGCG CTGAGATCGT GCGTGCACAG 900
GCCGGGGTGC GGCCGGCGTG AGTACGCCTG CGCGTGCCGC CATTTCCTGC AGCCGCAGAC 960
TCTGCCTGCG GTGCTCGCCG GGAAATGAGA CGATCAACAA AGAAAATGGT TGTTTTGGGC 1020
GAGATCGACC GTGGAGAGGC TTTTTCTGCA GCAGTCCCGG TTCCTGCCGC CAGATGGCGC 1080
TCGAGGATCA CAAATGGGTC TAGGGTTCTC ATAATGGCCC CGCCTAAGAA ATTTTGGATT 1140
CTCCTGGCCC TTCCCCCCTT TGTGGGGTCA 1170
|
