| Tag | Content |
|---|
EnhancerAtlas ID | HS078-17041 | Organism | Homo sapiens | Tissue/cell | H2171 | Coordinate | chrX:18892820-18894270 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chrX:18893442-18893453 | CCACACCCTGC | + | 6.62 | | USF2 | MA0526.2 | chrX:18893849-18893865 | GGAGGTCACGTGGGCC | + | 6.5 | | ZNF263 | MA0528.1 | chrX:18894132-18894153 | TTCTCCTTCTCTCCCTTCCCT | - | 6.09 | | ZNF263 | MA0528.1 | chrX:18894028-18894049 | GGAGGAGTGGTGGAAAGGAGG | + | 6.21 | | ZNF263 | MA0528.1 | chrX:18894145-18894166 | CCTTCCCTTCCCTTTTCCTTC | - | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGGCTGCTC TCGAACCCCT AACCTTAAGT GATCCACCCC CACCTCGGCC TCCCAAAGTG 60
CTGGGATTAC AGGCCTGAGC CACCGTGCCC GGCCGGCGTT TTGTATTTTT AGTTGTCAAC 120
TCTGGCAACC CTACATGGAC TTTGAAGTCA TACAACCTGA TTTCAGATGC CCCTCTGCCA 180
TCAAGGGTAT GGGAAACTCT GGACAAATGA CATGGGCATT CGGAGCCTCC ATTTATCGTA 240
ACCACAACCA CATCCCGGGA CCATAGCAAA GATGAGAGCG AATGTACGTG AAGCACGTAG 300
CACAGGAAGC GGTATCTCGT TGTAGTGGAA GCTGTTGGCC CCGCTGCATC CCCTTTATTG 360
GCCGGTGCAC TCATCCTCCA GCTTCTAGGA ATGTTGGGTG CCAGCAACGC ACAGCGACCC 420
CCTTTCCTGG TGCATTGCCC TGGACTGATG GGAGGTGCTT GCCTAAGAGC TTGTGTCCCA 480
TCCGCGTCCC CCCCAACTGC CCCCATTGCC ACCCGCGGGC AGCCAGCAGT CACTGGCTAA 540
CTGATGGCAG AGGCTGCTTT TATCTTGCAG TGCTCACTCC AGAGCCCCCT GTGGCGTCGG 600
GCTGGCTGGG TTCCACCTGA TGCCACACCC TGCTCAGCTC CTTCCCCTGT CACTCTTGCT 660
TCCTTCCAGG CTGCTCCCTG GAGCACACTC TTGGCATTTC ACTTGTACAA CATGCCTGGC 720
CCTGGCACGC TGCTGGTGCT GGTGTGCACA CTGATCACAT AAGCTTGTGA GCATTCAGCG 780
CTGAAGGCCA AGGATGCCTT GTGCTCTGAG AATGGGATCT GCTTGGGGGC AGGAGAGACT 840
TGGGGTCGGG GTGCGTTGCT GGGGAACAGA CAAGGGATCT GTCGCCTCCT GGGAAGCTGG 900
GAAATGGTGT GGGGTGGGGC GACTGGGAGA GGACGGCCAG GGACAGCTTC AGGCCTGGTG 960
TCCTGCAAAA CCTGACACCT AGCAGATGGG AAGATGCGGC TCAGCTACCT CCTCCCGGAG 1020
CCAGGCTGAG GAGGTCACGT GGGCCCAGGA GGTTCAGCCT CAGTTGGGCT GTGCTTGGGG 1080
AAATAAATCA TCAGGACTCA ATGCAGAAAA ATGACATGAA TTAGGGGGCT CGTCTGGGTG 1140
CCACGCGAAC CTCTCCCTGT CTCTCCACCT TGCAGGCATG CTTTTGGGTA CCGACACATG 1200
TTCCTCCAGG AGGAGTGGTG GAAAGGAGGA ATCCTTTGGC CTCCAACCCT GGAAGAAGGT 1260
GTATAGTTTT AAAGGGCAAG GCTTGGCTTT GAATTGCAGC TCTGCCACTT CTTTCTCCTT 1320
CTCTCCCTTC CCTTCCCTTT TCCTTCTCTT CCCTTTTCCT TCCCTTTCCC TTTCCCGACA 1380
GTCTTCTCTG TTGGCCAGGC TGGAGTGCAG TGATGCACTC TCTGCTCATT GCAATCTCCA 1440
CCTCCCCGAG 1450
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