| Tag | Content |
|---|
EnhancerAtlas ID | HS105-84356 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chrX:16804710-16806100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chrX:16805151-16805162 | GGGCAGGTGCG | - | 6.02 | | ZNF263 | MA0528.1 | chrX:16804858-16804879 | GGAGCAGGTGGGGGGGGGTGG | + | 6.1 | | ZNF740 | MA0753.2 | chrX:16804865-16804878 | GTGGGGGGGGGTG | - | 6.09 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chrX | 16805200 | 16805600 | | chrX | 16805192 | 16805460 |
| Enhancer Sequence | AGGTCAGTCA GGGGGACGCC CTCGTTGTTG TCGGGCCCGG GGGATGTTTG GGCTCCCTTT 60
TTCAGGGTCC ACCTCTTCTC TCTCCCTGGT TACCTATAGC CACGGGACGA ACATCCGGTC 120
TTCTTCCCTC CCGGGGGTGA CGACAGTGGG AGCAGGTGGG GGGGGGTGGG ACCGCGATGG 180
ATGGGGTGGG AAGGGACGAC GGTTGGGGTT TGGCGGCGCG CGGCGGGGAA GCCGGGAGGG 240
AGGGCAGGGG GCGCACGCGG TTCTAAGGGA GAAGGGGTGC GAGGCGGGGG TGCGCCAGGT 300
GTGACAGCCA CGTGCGGCCA GCACCGCGGG GATCCGGGCG CCAGGCGTTC CTTCTCCCAG 360
TCACCGCCGT CACCGTGCTC CCGGCGCTGA GCGCCGCCGT CCGGGGGCTC GCTGGGGTCG 420
TGGGCTCGCC CTCCTGGCGT CGGGCAGGTG CGCAGGGCGC GCTGCGGGGT GCCCCCGGGC 480
TGCTCAGGCT AGGCTGTTGC GCAGTAAGAT AACCGCGCGG GAGCCGGGGT GTGCTTGGCC 540
CCCCTTCCCC CGCCCCCCTG CGCTCCCCGC CACTGCGCGG GCGGGCAGGC GAGCGGGTGA 600
GTGTCGCAGG GCCGGTGCGA GCGGGACGCT CGGCCCCCGG GACCTAGACC CCGGGGCTCC 660
GAGGGCTTGG CTGCACGTGG GGCCGGGGAT GGATGGGGAG GCGATGCTGG AGGACCTCGG 720
TCCTGCAGAG TTGGGATATC GCATGATAGC TGGTCCTCCC AGTCCTATTT ACCACCCTCC 780
TCTTTTTTCC CCTCTTTTTT TTCTTTCATT TATTATTTTT TTAATTTGAT GAGTGGAAAC 840
TTGAATGCCT TCCCGACCCT GGCCTTGGGT CTTTCTTAAT CTGGGAAACA GGCCGGACTG 900
TTCCCCTTGC CTTACTTGAC TCACGTCAAG GAGTTTTCAG TCCCTCCCTA GATACAGGAA 960
AATTGAGACC TCTTTCAGAA CGGGACAATT CCACTTGTTC TGGAGCTCAG TGGGTGGAGT 1020
TTGAAAAAGA TTGCACAACG AACGGGGTAC AGGGTTTTCG GGGCCCTGGA ATGGATAATT 1080
GCGGGGACTG AGACTGGGAA GGTGGGAACC CCATCTCTTT TTTTCCTTGC AGGTGAACAT 1140
ACTGAAACGT TCGACTTGTT GGATATCTTG CTTGATCACC GAGGGCTATT TAATATTACT 1200
TAATTATGTA TTTGAACACT CTTAACTCCT GTATGAAATT ACGAAATAAT ATTTTTCTAA 1260
TGCAATTCAT AAACTTCAAA TGGGAGAACA AAGGTCCAGT TTACGTCTGA GCAGAGTGTT 1320
AAGAATTAGC TTTTTGGGGC CTGTTTCTAA GGTCAGGTAT TTTCATGTTT CTGCATGACA 1380
GTGTTACTAC 1390
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