Tag | Content |
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EnhancerAtlas ID | HS048-11123 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr14:30070310-30071620 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NR2C2 | MA0504.1 | chr14:30071465-30071480 | GGAGGGCAGGGGTCA | + | 6.26 | TFAP2A | MA0003.3 | chr14:30070535-30070546 | TGCCTCAGGCA | + | 6.02 | ZNF410 | MA0752.1 | chr14:30070887-30070904 | GAGTATTATGGGAGGGC | - | 6.97 |
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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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Enhancer Sequence | ATGAAATTTA AAACCTCAAA TGGCTCACTG CTCAGAAACC TCACAGATGG ATGCTGGGTG 60 GTGAGCAGCA GAAGGGGTTG TGGGTGAGTC TACATTGTTG TAGTTGTCCT CTCACTACCC 120 ATTTGCAAGG AAAGCCTGGC ATCAACTGGA TATAGAACCA GGAGCTCTGA TGATGATAAC 180 TCATTTCTTA GAGAGTCCTT TTTCTACTTT GCCTGTTTTG ATCTCTGCCT CAGGCATCTG 240 ATGGGTCTCT TTGATTCTGA TGCCTTGGGT CAAATCATAC AGCATAATGG AGTCATGGAA 300 TTGCAAGTTT ATTATGAATG TGATCTGAGC AGACGCCTAC ACATCTACCC AATAGCCTTT 360 AACCTCTAAA GGGCTAGAGT CATTGTTCTT CAAACCGTTG CACTGTTAAC TGGTCAAGTC 420 TGGCAACTTC GAATAGACCT CACCTCCCAC GTTGCTCTCT CCTGGTCAGA GCTGAAGCAC 480 ATGGAGATAG TTGGGGTTCA CAAAGCTCAT ATTATCAACC CTCTTACTTT ACTTTTCCTG 540 ATTACTTGCA AATAAGAGCA GATAGCCAGA TGGCTTTGAG TATTATGGGA GGGCCAGAGG 600 CTAAGGAGGC GACTAATATG ACGACATACA CTTGTTTGAT AGGCACTATG GAACATGTGA 660 TAGTATTGTT CATACTTGAA CTTGTGTCCC AGGCTGTCTC ATTTCCTTTT CCTTACATGC 720 CTTTCCCTGT TAGAGAAGCC AGACTGACTG CACAGACCAC TGGCCTCTGA AGTGTCAAAG 780 GTCTCAGCTG TTCTCTTTTA ATCAATAATC ACAGCACGAG CTTTAAGGAT TACATGAGTT 840 CGGCTAGAGT TCTGATTCTC CTAGGACAAG TCCACTATGA TATGTGCAAA GTACACGTTC 900 CTCTTTGAGC ATCTTCATTG ATTCTTTTAT TTTTCTATTT AATATAACTG TAAGCACTTA 960 AGCAGTGTTC TGGGGAGTCT GGCTTCCTTA AATGGCTAAG CTTTGCAGTA CGGGTGGGAA 1020 GCAGAAGCAA TGAATCAGAA AGGAGCAGAG CAACAGAAGT AGACAGGAAG GGTAGGTGTC 1080 CTCTGTGTGT AGGCAGACGA AAAACTAGTA GGAACAAGAG ATAAGCGTTA AGGGAGAGTG 1140 ACCTCGGGGG CCCAGGGAGG GCAGGGGTCA CGGGAGTAGT ATTGGAGCTG CACAGCCTGC 1200 TGCTTCTGCT GATCTTAGAT TCTGAAAGTT GGAGAAGAGG GGAGAGACGC AATGACTGGG 1260 GAGTCCTCCT ACCTAAATTA TCTGAATGAT ATGAATCCTT ATGTGCCTCT 1310
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