Tag | Content |
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EnhancerAtlas ID | HS076-25037 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr17:44203720-44205130 |
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) |
TCF7L2 | MA0523.1 | chr17:44204506-44204520 | AAAGTTCAAAGGAC | + | 6.12 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr17 | 44204602 | 44204656 | chr17 | 44203802 | 44203941 | chr17 | 44204705 | 44204745 |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I046123 | chr17 | 44200637 | 44203769 |
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Enhancer Sequence | TCACTCGAAC CCAGGAGGCG GAGGTTGCAG TGAGTCGAGA TCGCGCCATT GCACTCCAGC 60 CTGGGTGACA AGAGTAACTA CGTCTCAAAA AAAAAGTAAA AGTCTCCATC TTTCCACTAG 120 ACCACACTGC TTTTCTCAAT CTTTATGACA AACATGTAAG GCATATTGGG TTCTGGATAA 180 TATGTCAAGG AGATATACTA TTTTGGAATA TTTTGGCAAA TAAAGGGGGG CTTTAAAACA 240 TGAAATTTTT TTTTCTTAAT AAGAACTGTA ATCTATTTCC CCAACTTCAT TATTAAGTGA 300 GTTTTAGGCC TAGGTCTTCC AGAACAGTTT CCTCCAAAAC ATACAGTGTA ATATCTGGTT 360 ACTCTTTATG TGTGCATAAG AAATGTCACT GTGACAAATG TTATAAAGAA AAAATTTGAT 420 TACCCTAAAA ACAAATACAT AAACAGCCCG CAAGTTTAGC TCCTAAAGTA GGAAAGAATA 480 ATGTGAAAAT GTTTCTGGCT GTACCACTCA ACAAAAATTT GCCCGCCAAT AAGGAATCCT 540 TTCTTCAAAA ATTGGTCATG ATCATTAGCC AAACTGTAAC CAGTAACATC CAGCTGGATT 600 ATGGAGCTAA TAAAGAACAA CAGAGGGGAT CCACAGGAAA TTCAACAGGT AATTTACAAC 660 TGGCTCTCTC ATCAGACTGG CAGACTGGGT CTAATCCAAG GTCAGATGAC ATGGGGGATT 720 ATGGAAGCCA ATAACAATCA TATTTAAATA AATGTCCTTT ACAGAACATC ACCACTTTCC 780 TCATAAAAAG TTCAAAGGAC TATTTTCACC CCTCACAATT ACAGTAAGGA TAAGAAGCCC 840 AAGCACAGCT TGAAGCAGCA AAATTTTCTG AAAAGGAATT GAATTCTGTG TTCTCTTCAG 900 GATCTTCCTT TCCCAATAAT GGGGGTATTA AATTTCACTT ATAAATCAAA CTGAAAGGGA 960 AAAAAAGAAC AATAAAAAAT GAGCTGGAAA ACCTACATTC ATCATCTTCA AAACAACATC 1020 AAGTTAGAAA CAGTTTTAAA GCAATGTTAC AACTCCTTTA GAATCTGGCA GGTTTTCTGG 1080 TTTTTACCAG ATCCCGCTCC GGCAACAACA AAAAAAGAAA CAGTTTTAAA CAGTTTTATG 1140 GGCGTGGTGG CTCACACCTG CAATCCCAAC ACTTTGGGAG GCCAAGGCGG ACAGATTGCT 1200 TTTCAGCACA AGAGTCTGAG ACCAGCCTGG GCAACATGGT AAAATTTTGC CTCTATAAAA 1260 AAATACCAAA AAATACCAGG CATGGTGGTG GCACACTCCT GTAGTCCCAG CTACTTGGGA 1320 GGCTGAGGTG GGAGGACTGC TTGAGCCCAG GACAGCAAGG GTGCAGTGAG CCGAGATTGC 1380 ACCAATGCAC TCCAGCCTGG GCAACAGAGC 1410
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