Tag | Content |
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EnhancerAtlas ID | HS103-04648 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr11:102244980-102246260 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXA1 | MA0148.4 | chr11:102245446-102245462 | CTTTGTTTACCTAATC | - | 6.09 | MEF2C | MA0497.1 | chr11:102245031-102245046 | ATCTATTTTTGGTCT | - | 6.45 | NR2C2 | MA0504.1 | chr11:102245210-102245225 | GGGGGTCAGGGGTCA | + | 7.06 |
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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 |
GH11I102374 | chr11 | 102245532 | 102246131 |
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Enhancer Sequence | TTTAGAGTTT CCAGCTTTTC TGTTCTGTTT TTCCCCCATC TTTGTGGTTT TATCTATTTT 60 TGGTCTTTGA TGATGGTGAT GTACAGATGG GTTTTCGGTG TGGATGTCCT TTCTGTTTGT 120 TAGTTTTCCT TCTAACAGAC AGGACCCTCA GCTGCAGGTC TGTTGGAATA CCCTGCCGTG 180 TGAGGTGTCA GTGTGCCCCT GCTGGGGGGT GCCTCCCAGT TAGGCTGCTC GGGGGTCAGG 240 GGTCAGGGAC CCACTTGAGG AGGCAGTCTG CCGGTTCTCA GATCTCCAGC TGCGTGCTGG 300 GAGAACCACT GCTCTCTTCA AAGCTGTCAG ACAGGGACAC TTAAGTCTGC AGAGGTTACT 360 GCTGTCTTTT TGTTTGTCTG TGCCCTGCCC CCAGAGGTGG AGCCTACAGA GGCAGGCAGG 420 CCTCCTTGAG CTGTGGTGGG CTCCACCCAG TTCGAGTTCC TGGCTGCTTT GTTTACCTAA 480 TCAAGCCTGG GCAATGGCGG GCGCCCCTCC CCCAGCCTCG CTGCTGCCTT GCAGTTTGAT 540 CTCAGACTGC TGTGCTAGCA ATCAGCGAGA CTCCGTGGGC GTAGGACCCT CCGAGCCAGG 600 TGTGGGATAT AATCTCTTGG TTCGCCGTTT TTTAAGCCAG TCTGAAAAGC GCAATATTCG 660 GGTGGGAGTG ACCCGATTTT CCAGGTGCGT CCGTTACCCC TTTCTTTGAC TCGGAAAGGG 720 AACTCCTTGA CCCCTTGGGC TTCCCAAGTG TGGCAATGCC TTGCCCTGCT TCGGTTTGCA 780 CACGGTGCGC GCACCCACTG GCCTGCGCCC ACTGTCTGGC ACTCCCTAGT GAGATGAACC 840 CGGTACCTCA GATGGAAATG CAGAAATCAC CCGTCTTGTG CGTCGCTCAC GCTGGGAGCT 900 GTACACCGGA GCTGTTCCTA TTCGGCCATC TTGGCTCCTC CCCTCCTTCA ATAAATATTT 960 GTTGAGCATG AGCACCAGTG CCAAATACTG TGCCTAATCA CAGTGGTTGC TGTCAAGGAG 1020 TATATACACT AGCTGGCGAG ACTAGTGTGC AAAAGACAGG GTTAAAGGGC CAGCAGAGAG 1080 GCGAAGGTTG CATATGTATT GGAGTATTGC GTTGGAAGAT GCTTTCTTTT TAAGCTTGTA 1140 AGTAAAGACA GGAATAACTT AAGAGTACCT TATTGCATGA CCGTGTAGCA AAATATTTAA 1200 AGTCTGGACT TCTACATTGA AACAGATTTG TGTTTAAATT CTAGCTCCAG GCTGGGCGCG 1260 GTGGCTCATG CCTGTAATCC 1280
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