Tag | Content |
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EnhancerAtlas ID | HS034-31678 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chrX:69653550-69654700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chrX:69653806-69653825 | TAGCTCCACCTTGTGGCCG | - | 7 | SP2 | MA0516.2 | chrX:69654309-69654326 | ACAAGACCCGCCCCCCA | + | 6.28 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH0XI070433 | chrX | 69653051 | 69655901 |
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Enhancer Sequence | ACGAATGTAA TCTCCATTTG GTCACAGCCT AATCTTTTCG GCCCAGGGGC TGGGGAAAGG 60 AGGCACCTTC CATCTACGGT TGGATGGGAC ACGACCTTGA GGGGCCATCA GGGGGAGATG 120 GGAGGAGGTG GGTTGGAGGT GGGAGGAGAA TCACCTGCGG CAATGAAGGA CTCGCGGGAG 180 GCTCGCGGGA GGCCCGCAGG AGAGCAGCCA CCTCGGGGGC GTCCGGAGGC CGGGCGCGCG 240 GTGCAGGGTT GCACTGTAGC TCCACCTTGT GGCCGCCCCA AGAGGAGGGC CGCATCCGTC 300 GTCGCCGTGA CGTATTTGCT GAATGCCACC TGTTTTCCGT GCCGCTTGGG GACTCGTGTC 360 CTTGACTCAG GACTCCGAGG GCAAGGTCCG ATTTCCACAA GTTTTCGCTC CTCTGGGCTG 420 CGCGCAGGGT CCAATTTCCG GCCCAGCCTT CCCTTGGAGG AGCAAGTTCC CCAATGTGTT 480 TGCGGCTCGG GAGTCCCTGG GCTCCGCAGC TAAGGTGGCC AGTGCGGAGC TGACGGAGGA 540 TGAAGAGTCT AGTAGAAGAA GGGAGGGGCT AAGCCAAAAA TGGGGACAAG AGGGGCTCTG 600 TGGTGACCCC ACAGTCTTCC GCCACACCCA CATTCGACCT AGTTCGTATC TCCACACGGA 660 GGGAAGTAGA ACTAAGGAGT CGGCCAGGTA GGGAGGTCGG GTTCTCGGTT CCTCCTCTCT 720 CGCCAGACTG GGACCTGGGG CAGCACTGGC ATCCTCGGGA CAAGACCCGC CCCCCACCCT 780 CGGTTGCCGG GCAGCCGCGG GAACTACAAT TCCCAGTGAG TCCCCGGCCA TTTCCGGTAT 840 CTGGCTGGAC GCAGGCGAGT TTGAATCCGT GTTCCCGCCC CCTTCTCCCG GGCCCACCCC 900 TTTCCTTTCT GGCCGCCCCG CCCTCTCCGT GCGCATCCCT GCACACTCCG GCTCCGGAGG 960 CCGGCCGCGC CCACGTACCT GACCTGCAGC TGGCGCGGTG GGCGGGGGTG CCAGCATGCG 1020 ACGCACGGGG AGGCTGGAGG CGCGCGGAGA GCGAACGCCG CAATCCGGTC CTGGTCCTGG 1080 TCTTCCTGGG AGTCCACGCC GCTGTGTACC GGGCAGGTCT CTCCTACACT CTGCCTTTTC 1140 GAGCAGCATT 1150
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