| Tag | Content |
|---|
EnhancerAtlas ID | HS012-18099 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr3:48934280-48936120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DMRT3 | MA0610.1 | chr3:48935688-48935699 | AATGTATCAAA | + | 6.02 | | EWSR1-FLI1 | MA0149.1 | chr3:48934300-48934318 | CCTTCACTCCTGCCTTCC | - | 6.47 | | HINFP | MA0131.2 | chr3:48936038-48936050 | CAGCGTCCGCGC | + | 6.22 | | HNF4G | MA0484.1 | chr3:48935336-48935351 | TGGACTTTGGTCCCC | - | 6.39 | | Mafb | MA0117.2 | chr3:48934605-48934617 | AGTCAGCAATTT | - | 6.92 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr3 | 48935999 | 48936096 | | chr3 | 48934891 | 48935000 | | chr3 | 48935000 | 48935200 | | chr3 | 48934400 | 48934409 | | chr3 | 48934539 | 48934759 |
|
Enhancer Sequence | CCACTTGCAA GCCACACTCA CCTTCACTCC TGCCTTCCCA TCAGACTGTC TGGGTCTCCC 60
TACTCCTTCA GTCTGAACTC ACCCAGCACT TGAATGCCTG TTCTAACGCA CCACCTTCCA 120
TAGAGCCTTT TCATGACCCA CTCTGAAGCG CTGCAGCTTT TGCCTTGTCA GGACACACAG 180
CCCACAGCTC AGTTACACTA TCTTGGACTT CTTTTTTTTC TTCTTCTCCT TTTTTTTTTT 240
TTTTTTTAAC CTTGGAACTC TGAAAGTACC TTAAGGTCAG GCTTTGATTG GAGCCCACCC 300
AGCTCACTAA GGCCAAAAAC ACAGCAGTCA GCAATTTGTG GTTTTGGTTT AAGCTAAAAA 360
GAGGCTTTCT GGTTGCTAAA TATGCCAGTG AGCATTTCAG TTATTTGCAC TTCAGTGCAG 420
AGGTCATCCA GTCCTTCTTG GGAGTGACAT CAAGGACAAA GGTGATATGG AGGTAGGAGC 480
AATATTTGTG TGTGTGTGAA TATATATATA TATATATATA TTTTTTTTTT TTTTTTTTTT 540
AAGGGCGGCC CCAGAGGCCT AGAACTAATA AGATATCTGC CTATATGGAC CAAGAGCAGG 600
AAGAAAGGCC AGACAATCGT CCCTCAGTAG ACAGTGCCGC TTGGAATGAC CACAGTCTGG 660
GAAGCACTAA CACATGGCAT TTACCACCAG CTAAATAAAC ATTTGATTTC ATGTTGCACA 720
ATGACCTAGC CAGTCCAGCT ACTTTAACCC TGGTCTTCCT ATAGAATGAC CCCAGTATGA 780
GCTCTACTTC AGGGCAGCTC CTCTCTTGGA TGAAAGGCAG CAAAGAGCTT GCTGCCCAAG 840
CTGGCCAAGA GGAAGTGCCC ACAAAACTAT TTCGCTGTGG AAGAAATCTG ACCCAACATC 900
CTAACAAACC CCCTCACATG GGCTTCCAAT CTTTTAAAAC TCATGTCTGC TCCCCACAGG 960
CCCACCCTGG CAATGACTTG TCAATTTCCT TCACGTCTAC GTCTAGAAAA AAAGTGAGAA 1020
AACTGGATGC AGCTTCGAGT GCTAAGCCAT GGGGGATGGA CTTTGGTCCC CAAGCAAAGC 1080
ATTAATGAAG GTGTTGCAAG GGGAATAGTT GAGATATGAT ATGAGGAAGA CCAGAGAACA 1140
ATTCCTGATG AACGTCCTCC CTCCCAAGCC TCAGTCTGAC CATAGCTTCC TCATCTGGGA 1200
GTTGTGAGAA TGAGGCTGGC CTTGTGCAAA GCTGATCACC TTGCTTTCCG TGGAAGGGGC 1260
TCGGTCACTG AGGTCATCAT TGCTTCTCAC AGGGATGCCT CTGCCCAGGA GGCTGAGCAG 1320
GCCACCGTTG GGTGACAGGC CGAAGAGTGT CAAGTATCTC CCCGGGCCGG GAAAGGTGCG 1380
AAAGAGATGG GTACTCTTGC CCCAGGGGAA TGTATCAAAG GACACCTCCA GAACAACCGT 1440
ACCGCTCTGT CTTTAGTTGT CTTCCTGGGG CAGGCTTTAC AGGGGACCTG TTTCAACCTT 1500
AACGATAATA TTAGTGTTGG CTGAAACCAA AACTATGGAG AGACGTTTAT TCCTTCCCAT 1560
CCCTAAAGAA GTGGCGCAGG GTCAGAAGAG ACTGCGGGAC AGGGAACTTT ACATCAGAGC 1620
TCTTGACAGG CAGTTAGAGG CTGCTCACTT TGCGCCGCCG CCTGGCTCTT TGGGGCGCAA 1680
GGTACAGCTT CCTGCCCACC CCTGAAAGAG AGATTCCCTA GACTTCTCAC GGAAGCTCAC 1740
ACATGCCCCT CTTCTGCCCA GCGTCCGCGC CTCGCGGGGG ACCATGCTTT CCGCGCCCCG 1800
CCCGGGCCTC CTCCCCAAAG CCTGCGACCC AGCCTCCCGC 1840
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