Tag | Content |
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EnhancerAtlas ID | HS129-04478 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr10:19001530-19002520 |
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 | GTGATATAAG AACACAAATA GGATTATGCC ACCCTCTGCT TCAGACTTTC TTTTGGTTTT 60 CCTTGAATTT AAAACCCAAA CTTGGCTGGG CATGGTGGCT CACGCCTGTA ATCCCAGCAC 120 TTTGGGAGGC CGAGGTAGGT GGATTGCTTG AGCCCAGGGG TTCGAGACCA GCCTGGGCAA 180 CATGGCGAAA CCCCATGTCT ACAAAACATA CAAAAATTAG CCGGGTGGGG TGGCGTGCAC 240 CTGTAGTTTT GGCTACTTTG GAGGTTGAGT TGGGAGGATT GCTTGAGCCT GGGAGGTGGA 300 GGTTGCAGTG AGCTGAGATT GCACCACTGT ACTCCAGCCT GGGGGACAGA GTGAGAACTT 360 GTCTCAAAAT AACCCCTAAC CACCCCCTCA GAAAAACTCC AAACTCCCTC ATTTGTGCTA 420 TGAAGCTGAA AAAAATGAAC CCTTTCTCAC CATACCTTCC TGTCTGAATG CTTCTCACTG 480 TCATTAAACC AATCTTGACC CGGGCTCTGA AGGCCTTTGA CAATCTACAG TCACAAACGT 540 GGCTTAGAAG TCCAAAGTTG AGTACAGGTG ACATAGCCAC TGAATCCTGT TCTGAAAACC 600 AGACGTTGGT GGAGTTGGCA AGTTAGCATG TTTGTCTGAG TCAGTATCAC TTGAACTAAT 660 TAAGTTTTTC TTTGCTCACT ATGCTTTGCT GGGCTTTCTC AAGCTTTTTA TGACTCATTG 720 AAATACAAGC TTGTGGTTCT CTTACGTTAC ATAATAGATC GGCATGTCAG CAGATAACTT 780 GTTTGCAGGG AGCTGGTGAA ATGCCGGGAC AAGTGACAAC TGCTCAATGT CTGTAAGGAA 840 CACATCACCA AATAGAACAG GTTGGAAAAT GAGTACAGAT ACTCGAAAGC CTTAATCTGC 900 AATTTCTAGG TCATCATGCG GAATGGATTA ATATAAAAAT GGAGAGTGGG CCTATTACTG 960 AGAAAAAAAT ACATCAGGAT ATTCCTTTTG 990
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