Tag | Content |
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EnhancerAtlas ID | HS101-04763 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr10:19001500-19002500 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIL3 | MA0025.1 | chr10:19002273-19002284 | ACGTTACATAA | - | 6.32 | RREB1 | MA0073.1 | chr10:19001902-19001922 | CCCCTAACCACCCCCTCAGA | + | 7.16 |
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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 |
GH10I018712 | chr10 | 19001394 | 19002565 |
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Enhancer Sequence | GCCTCCCTTC CTAGTAGAGT ATCTGTTTGT GTGATATAAG AACACAAATA GGATTATGCC 60 ACCCTCTGCT TCAGACTTTC TTTTGGTTTT CCTTGAATTT AAAACCCAAA CTTGGCTGGG 120 CATGGTGGCT CACGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAGGTAGGT GGATTGCTTG 180 AGCCCAGGGG TTCGAGACCA GCCTGGGCAA CATGGCGAAA CCCCATGTCT ACAAAACATA 240 CAAAAATTAG CCGGGTGGGG TGGCGTGCAC CTGTAGTTTT GGCTACTTTG GAGGTTGAGT 300 TGGGAGGATT GCTTGAGCCT GGGAGGTGGA GGTTGCAGTG AGCTGAGATT GCACCACTGT 360 ACTCCAGCCT GGGGGACAGA GTGAGAACTT GTCTCAAAAT AACCCCTAAC CACCCCCTCA 420 GAAAAACTCC AAACTCCCTC ATTTGTGCTA TGAAGCTGAA AAAAATGAAC CCTTTCTCAC 480 CATACCTTCC TGTCTGAATG CTTCTCACTG TCATTAAACC AATCTTGACC CGGGCTCTGA 540 AGGCCTTTGA CAATCTACAG TCACAAACGT GGCTTAGAAG TCCAAAGTTG AGTACAGGTG 600 ACATAGCCAC TGAATCCTGT TCTGAAAACC AGACGTTGGT GGAGTTGGCA AGTTAGCATG 660 TTTGTCTGAG TCAGTATCAC TTGAACTAAT TAAGTTTTTC TTTGCTCACT ATGCTTTGCT 720 GGGCTTTCTC AAGCTTTTTA TGACTCATTG AAATACAAGC TTGTGGTTCT CTTACGTTAC 780 ATAATAGATC GGCATGTCAG CAGATAACTT GTTTGCAGGG AGCTGGTGAA ATGCCGGGAC 840 AAGTGACAAC TGCTCAATGT CTGTAAGGAA CACATCACCA AATAGAACAG GTTGGAAAAT 900 GAGTACAGAT ACTCGAAAGC CTTAATCTGC AATTTCTAGG TCATCATGCG GAATGGATTA 960 ATATAAAAAT GGAGAGTGGG CCTATTACTG AGAAAAAAAT 1000
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