Tag | Content |
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EnhancerAtlas ID | HS102-13078 |
Organism | Homo sapiens |
Tissue/cell | HuCCT1 |
Coordinate | chr2:112789460-112791100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NEUROD2 | MA0668.1 | chr2:112789854-112789864 | GCCATATGGT | + | 6.02 | RARA | MA0729.1 | chr2:112789638-112789656 | GAGGTCGAAAGGACAAGG | + | 6.97 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 112789561 | 112789661 | chr2 | 112790543 | 112791081 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I112030 | chr2 | 112788379 | 112791976 |
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Enhancer Sequence | ATTGGCAAAC TCTCATACTG TCTTCTGAGC ATAAACTGAA AACAGCGTTT CAAATTCTCT 60 TTCATAGAAA CTCAAATTAC TTTTGTAAGT GGCTCTTGTA GGCAAAAAAA AGGGAGAGAG 120 GAAACAGGAA GAAACAAGTC GGGTTAATTG TCTTAACCGT GCTGGGGCTC AGGATCAGGA 180 GGTCGAAAGG ACAAGGAAAC AGACATATGC CAGAAGCACT CGTGACTGGC ACGTTGAGAC 240 TTGCCCTCCC TTGTGAGGAT TTTCTTTCTT TTGTGTTGTT TTTTTTTTCC TTTCTGTTGC 300 TTTTCTTAAT GAGTAGAAAT GAGAATCAAG CGTCAGGGCA ACTCTTGGAA AACAAAAAAA 360 AAAAGACACC AAAGCACTCT TCATGGTGAG CCAGGCCATA TGGTCAGAGG TGGGCTGGAT 420 AGGAGCTCAC CCTGCCAGAT GTCCTTGGGC AATCGTGGGC AGGTCACTTG ACTTTCCTTG 480 AGCCCCAGTT TTCTCAAGTG TTCAGTAAAC ATACCAATGC CTTTTTCTGC AACACCCTGT 540 GTAAGAAGGG GAGGAGGCAA GGTCTTCGAA AGAATATTAT ACTCACAAGA GGCTGTTCTC 600 AATTTGTGGC ATCATTCCTT ATGCAGTGCA AACCCAGCAA CATTTGTCAT ATTCAAAATA 660 TTTTCAGCCA GGCGTGGTGG CTCACGCCTG TAATCCCAAC ACTTTTGATG GCCGAGGAGA 720 GAGGATTGCT TGAACCTAGT AGTTCAAGAC CAGCCTGGGC AACATAGGGA GACCCTGTCT 780 CTATAAAAAA TAAAAAAGAA ATTAGCCAGG GATGGTGGCA TGCAATTGTG GTCCCAGCTG 840 CTCAGGAAGC TGAGGTGGGA GGATCACTTG AGCCTCAAAG CTCAAGGCTG CACTGGGCTG 900 TAATCACACC ATGGCACTCT AGATGGGGCA ACAGAGCAAG ACTCCATCTC AAAAAAAAAA 960 AGAAAAAGAA ACATTTTCCC TGATTGTTTC ATCAACTCCC TCCAAAATAA ACACAGTCAT 1020 TCATAATTTG AAAAGAGAAA GAGATAGTAT TTCGCCTTAG CCAGAAACGC ACAGTTGGGG 1080 AAGTTCAGAG TGAAGGAGGA GGCCCTCAGT CCTCACCTCA AACAGCCACT GGGCTCAGGA 1140 GCTGGAACTA CCTTCCTCTT GTCTATCCTG GGGTTTAGCT ACTGATGATA CAAGCCTCAT 1200 TGCGCCTCTC CCCAATATGT GGGTTATGAC AAGCAATGGT GGCTTGCTTT ACCAGGAGCA 1260 TTTGGGGACA TGTGGTGGGT CAGAATGCTA TCCCAGGAAG GGGATATTCC CTCTCTGCCT 1320 CCATGTCTGC CAGACCTAGC AGAGGTTCCC CACCTGGGAA ATGGGCCAAA CCACAGTCTC 1380 TTCTTTTACA GAGCAGGCTG ATTCTAGCCA GACCAGTTCT GATTCATGAA AGTCAAGACT 1440 TTTGTAACTT TTCCTGGTCA ATGGCAAAAG CAAGTTGGAA CTTCTGCTGA GTCCGTGGGA 1500 AAGTAACTGA CCCAATAATA AACTAGCTAC AACAGCAACT TAACTTCTCT AAAGATGTTT 1560 AGTAACTGAG TGACAAATGA GAAAATGGGA AGTTTTGTTT TCTTTAATAA ATGTTTCAAT 1620 GATGCACAAT GTTCCTATCC 1640
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