Tag | Content |
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EnhancerAtlas ID | HS048-02563 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:160894560-160896080 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:160894626-160894641 | GAGGTCAGGAGTTCA | + | 6.22 | STAT1 | MA0137.3 | chr1:160894956-160894967 | TTTCCTAGAAA | - | 6.14 | STAT3 | MA0144.2 | chr1:160895863-160895874 | CTTCCCAGAAG | - | 6.14 |
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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 |
GH01I160925 | chr1 | 160895198 | 160895930 |
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Enhancer Sequence | GGCCAGACAT AGTGGTACAT GCCTGTAATC CCAGCACTTT GACAGACTGA GGCAGGTGGA 60 TCACCTGAGG TCAGGAGTTC AAGACCAGCC TTACCAACAT AGTGAAACCC CATCTCTACT 120 AAATACAAAA ATTATCCAGG CACGGTAGCG CATGCATGTA ATCCCAGCTA CTTGGGAGGC 180 TGAGGCATAA GAATCACTTG AACCTCAGAG GCGGAGGTGG CAGTGAGCCA AGATCATGCC 240 ATTGCACTCT AGCCTGGGCA ACAAGAGTGA AACTGCTTCT CACAAAAAAA AAAAAAAAAA 300 AAAATTATCT TAGGTCCTCT CGTGTGTGCA TCAAGAGTGG CAAGAAGACA AAATGAAGAA 360 AATCAATTCA GTTGACTGAA AAGATAAAAA TATTTTTTTC CTAGAAAAAC AAGACCCAGA 420 AAGAGAAAAA AAAAAAAACA TAAAGGTCTT GTCAATATAC CTATAGCTTG AATATCTGCT 480 TTTAATTAAG TTGACTTTGA ACCAAATATC TTATTACAAG ACTCTAGCCA AAACAAGCAG 540 CAAATATTTC TTACCTTTGA ACTTTACCAA AGGCAACCTC CCAAGTGCTC AGAGAAAGGA 600 AAATTCAAGA CAGGAAGTCA GAAGTTGTTC ATGGAGGGAA AGAGAATCAA TAAATGGCAA 660 AAGTCACACA GATATCAAAC CAGAAAGTGT TACAACAGTG GGTAGCTAAT TAGGTATGAG 720 CAGGGCAGGA GAGGGCTCCC CACACACAGA CACACACACA CACACGCACT AGGAGTGTTG 780 GGCGCCAATC AGGTGATGGT CAGGCGGTTG TTAACTGTTT CCTTAAAGTA GTAATCATTC 840 ACAGCTGGTG CCAGGGAACA GCAGTCTCCT AATAGATACA AAACACCTGA AACTGATCAG 900 CAGCTTCCCA ATAAGATCTC AGGAGTTGGG AGAAGTAACA CAAGATCCTG GAAGGATGCC 960 AACGTATAAA ACCCCGAGTC AAGAGGTCAA GTTGTGCACT TGGTCTCTTG AGTCACCCAC 1020 TTGGCTTGTA TTTCCAAGTG TACTTTCCTT ACTGCTCTAA AGCTTTTTAT AAACTTTCCC 1080 TCGTGTGCTA AAACTTGCCT CAGTCTCTCC TTCTGCCTTA TGCCCCTCAG TTGATTTTTT 1140 TCTTCCCAGG AGGCAAGAAC TGAGGTTGCT GCAGACCCAT GTGGATAACT ACCACTGGTA 1200 AAAAAAGTAC TCATTCCCTA AGTCGGGAAT TGAACCCTGG CCACCACTGT GAAAAGACAG 1260 AGTCTTATCC ACTAAGCCAC AGCATCAGGC AGTTTCTGCT GCTCTTCCCA GAAGTAGCCT 1320 AGAGAGGTCA ATTTTGAACT TCAAATGGCT TTTAAATGTT CAAAATAATT TTCAGAGCTG 1380 TTACATGAAC TCCGAAATTC CTGTTCCCTG GATGATGGAG ACCAAGACAA AGTATTGCTC 1440 TATGGTTACA AGATCAATCT CCCAATGACA TTAAACAAGA AGATAGAGAA ACCTCATCCA 1500 GCTTTTTTGT TTCAGGGATC 1520
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