Tag | Content |
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EnhancerAtlas ID | HS158-25052 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr17:74413600-74414560 |
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) |
HINFP | MA0131.2 | chr17:74413894-74413906 | CAGCGTCCGCGA | + | 6.11 | TCF3 | MA0522.2 | chr17:74413865-74413875 | AGCAGGTGTT | - | 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH17I076417 | chr17 | 74413626 | 74413718 |
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Enhancer Sequence | TTGTTAATAT GGTCAAAATT CTCTACCCCC TCCTTTTTAT GAGTGTGGAC ACACCCACCA 60 CCAGTGATAA GAGGACATGG ATGGAGGCCA AATGAGAGTG CACTGGGTGG CTGAACTGAG 120 CTGGGTCTTT AGAGGCCATC ACTAAAACCA CCTGGCAGAG AGCACCACGA AGGGCCTTCG 180 ACTACAGGAG GAAAGAATGC TAAGCATGTC CAGGGGCAGG AAACAGCTAT TGCAGGCCCA 240 GGCGAGACAG GAGGAAGGGA AGAGGAGCAG GTGTTTGATG CTGCATGGAT GCATCAGCGT 300 CCGCGAAGAG ACGTCTGGGT GAAGAGATGA ATGTCTCACT GCACCTGCAG AATTGGGCAG 360 AAACTCCTCC CAGTCTCCAT GATGGTGCTG TTTCCGCTGG TATTTGAGTC CTGGCTCACT 420 GCATTTAGAG GAGCTGCTTG CTGCTGTTGT GCCTTGGGAG AAGTGGAGGT GGAGAAGTGG 480 GCAGATGAGG TTCAATGCTC TTCACCACCT CAGGAGGAAG GCGCAGGGGG AGGTCACAGA 540 GCTGGGACAC GTGGAGTGGG CCTACACCCA GTCCCACCCT GGGGTCTGGG ATAGCTGCCC 600 CACACTGCCC TGGGACGCCC TGAAGAAGGG ATAATAGAGA ACAGACACCA ACATGTGAGA 660 CCTGGAACCT CAGCCTTCTG ACAATGTTTT CTATACTATT AGGCAAAAAA CTTCCCTCTT 720 CTAGGAGCCC ACAGCCTCCC GGAGGGCTCT CCAGGCCTCA CACAAAAACT CATTTTATCA 780 CAGTCCTGAA GGAGGTACAC AATTCCTGAA AGTAACAGAC TAAACTGTAC TTGGACTATA 840 GGACACCCTC TTCCAGGAGC CATGCCTTAC AACCAGCAAC TGCGAGGCGC CATTTGGCTG 900 TCTGCACCCT GTGCTGGCCT CTGAAGGGCA ATGGTGGAAG CCAACAGTTG GAGGAAGTTT 960
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