Tag | Content |
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EnhancerAtlas ID | HS048-10421 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr13:47264930-47266670 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXF2 | MA0030.1 | chr13:47265216-47265230 | CAAAAGTAAACAAG | + | 6.16 | PHOX2A | MA0713.1 | chr13:47265454-47265465 | TAATCCAATTA | + | 6.02 | Phox2b | MA0681.1 | chr13:47265454-47265465 | TAATCCAATTA | + | 6.02 |
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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 |
GH13I046691 | chr13 | 47265141 | 47267042 |
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Enhancer Sequence | AATTATCTTA CATAGCTTCC TATTTTCACT TGGTTTGGCA AAGATTTTAC CATCTATGAT 60 CAGGTGATCT TACTTCCCAT TTAGATGACA TTGTGGGGTT CAGGGATCAC ACCTCATTCT 120 TTTTCTTTGG CTGCTGCCAT TGATTGATTT AGCATTTGTC ACTGAGAGAT TAAAAACATC 180 TTTTTATCAA GATAAACAGG AAAGTGTGGA GCTCTATGAA TATTTGTTGA ATGAATGAAA 240 TGCATGCCTA ATTTCTGCCA GTTTCTAAAC AATCTGTGCA TATGTCCAAA AGTAAACAAG 300 GACAGACTCT GAAAACCATA CCTCAAGAAC TTAGGAGCAA GCCACAATCT CCTGAAATGT 360 GTTTTGTGGA GGTTCCTGAT TTTTGAGATT TGGAAAGCTA TTTCCTAAGT AGCAACAGTA 420 AAATGGAGAC ATAGGAAAAT AAACCAGGCT CCATATTTCA GAATCATAGG TTTTCTGAAT 480 AAACGTCATC AGCTACTGTG GGAAAGGAAG CCCTCAGAGA GAACTAATCC AATTATTAAA 540 GCCGAAGCTT TCTTCCAAAA ATCACACAGA GCAGTTCTTT TTAACTACTA CAGTTGTTTA 600 GCATTTTTAT ATATGTGATG CAGCTTCCTC AGCCTAAAAC AGAGAAATAA AACAGGCACC 660 CGTATTAGTT CATTCTTGTG TTGCTATAAA GAAATGCCCG AGGGTCGATA ATTTATAAAG 720 AAAAGAGGTT TAGTTGGCTT ACAGTTCTGC AGGCTGTACA CAAAGCATGT GACCAGCAAC 780 TGCTACTGGC AAGGGCCTCA GGGTTGAAGG TGAAGGGAGT GCCTCCTGTC ACATGGTGAC 840 AGCCAGAGCA AGAAAGCAAC GAGGTTGGGG GAGAGCAACG GAGGAGGTGC CATGCACTTT 900 TTTTTGTTTT TTTAAGACGG AGTCTTGTTC TCTTGCCAGG CTGGAGTGCA GTGGCGCGAT 960 CTTGGCTCAC TGCAACCTCT GCCTCCCGGG TTCAAGTGAT TCTCCTGCCT CAGCCTCCCT 1020 TATAGCTAGG ACTATAGGTG TGTGCCACCA CGCCCAGCTA ATTTTTGTAT TTTTAGTAGA 1080 GATGGGGTTT CACCATGTTG GCCAGGATGG TCTCGATCTC TTGATCTTGT GATCCACCTG 1140 CCTCAGCCTC CCAAAGTGCT GGGATTACAG GTGTGAGCCA CCACGCCTGG CTGATGCCAT 1200 GTACTTTCAA ACAACCAGAT CTCACATGAA CGCATAGCAA GAACTGCATA GACCCTTCTT 1260 GAGGTATCCA CCCCCAAAAC CCAAACACTT TCCACCAGGC CCCACCTCCA GCATTGGGGA 1320 TTACATTTCA ACATGAGATT TGGAGGGGAC ATACATCCAA ACTGTGTATC AGTACCTGAC 1380 AAGATTTCAG CTTAAAACAG AGAGAAGAAA ACACAGAGAA GCCCATAAGT GTTAGCTCCA 1440 TGAATTTTCA CAATGTGAAC ACACCCGTAT AACCAGCTTC CAGTTCAAGA AACAGAACTT 1500 TACCAGCACC CCAGAAAGCC CCACCCCGAC CCCAAGAATA ACCTCTTCCT AATTTTAAAT 1560 ACCATGGATT AGTTTTGCAT TTTTTGAACT TACATAAGTG GAATTGACCT TTGTATCTGG 1620 CAACTTATAT TCAATATGAT ATTTGTGAGA ATCACAGGAT GTTGTTTTAT TACATAGCAT 1680 TCTCCTTATC TACATTGATA ACACTTCTCT TGAGTTAAAC AGTGCACTGT ATCTTTTTAG 1740
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