Tag | Content |
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EnhancerAtlas ID | HS003-42984 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr7:129209040-129210820 |
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) |
Foxd3 | MA0041.1 | chr7:129209472-129209484 | AAACAAACAAAC | - | 6.32 | HES2 | MA0616.2 | chr7:129209328-129209338 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr7:129209328-129209338 | GGCACGTGCC | - | 6.02 | LMX1B | MA0703.2 | chr7:129210761-129210772 | TTAATTAAAAT | - | 6.62 | Nr5a2 | MA0505.1 | chr7:129210127-129210142 | GCTGGCCTTGAACTC | - | 8.25 |
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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 |
GH07I129569 | chr7 | 129209123 | 129210534 |
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Enhancer Sequence | AAGAGAATGG CGTGAACCTG GGAGGCGGAG CTTGCGGTGA GACGAGATTG CACCCCTGCA 60 CTCCAGCCTG GGTGACAGAG CAAGACTCCG TCTCAAAAAA AAAAGTCAGC ATCATTAGTC 120 ACATGAAAGG CTCTTTAGGC CAGGCACAGT GGCTCATATC TGTTATCTCA ACACTTTGGG 180 AAGCTGAGGT AGGAGGATCA CTTGAACCCA AGTGTTCAAG ACCAGCCTGG GCAACAGAGT 240 GAGGCCTGTC TCTTAAAAAA AAAAAAAAAA AGTGACATGC CTAATAGTGG CACGTGCCTG 300 TAGTCCTAGA TACTCAGGAG GCTGAGGTGG AAGGATCGCT TGAGCCCACG AAGTTGAAGC 360 TACAGTGAGC CCTGATAGCA CCACTGCACT CCAGCCTGGG TGACAGAGTG AGACCCTGGA 420 TCAAAAAAAG AAAAACAAAC AAACAAAAAA GAAGGTTGTT TAAAGACTAT GGGATTCATA 480 AGTCCCCCCC AGCCATGTCG GCAAAAGCCA AACATAGAGA AAAGGTTATC TTGAAAGGAT 540 TTGTGCACAA GCCTCTTATC TAATGGAATG AATCCCCATG ACATTCACAG GAAACCCACT 600 AGGCTCTTGA GAATTTTATT CCAGCAGAAA TACTGCCAGC TTGGACTGAA AGGGAGAGAG 660 AGAGGATGAA ATGTAAGAAG GCTGTGGATC CCCAAAATTC TACTGGCAAG AAACAGGCTG 720 GTAAAACTAT TCAGCTGCAA ACACCAGCCA TGTTTCATGA AAAAGGAATG ATGACTCAGA 780 GGGCGAAGGT TTGAGCCCAG AGGGTGGGGT GGAGCCTTGA ACCACAGAGG ATCATTACCA 840 GGTCTGGAAA ACTAATGTTT GCCCAGATAG ATTTTTTTTT TTTTTTTTTG AGACAGTCTC 900 ACTCTGTCAC CCAGGCTGGA ATGCAATGGT GTGATCTCGG TTCACTGCAA CCTCCACTTC 960 CCAGGCTCAA GGGATCCTCC CACCTCAGCC TCTTGAATAG CTGGGACTGC AGGCACACAC 1020 CACCATGCCC AGCTAATTTT TTTTTTTTGT ATTTTTGGTA GAGACGGGGT TTCACCATGT 1080 TGCCCGGGCT GGCCTTGAAC TCCTGACCTA AGTGATCTGC CCACCTTGGC CTCCCAAAGT 1140 GCTGGAATTA CAGGTGTGAA CACCACTACT CCTGGCCTGC CTGGATAGAT TTTGAAATTG 1200 TATGGGACTG ATGCTTCCTT TTTTCCTTCT GTTTTCTCCC TTTTTTGAAT GGGAATGTCT 1260 ACAATTGCTA TTTTATGGCT GTCTCAGCAT TGTATCTTGG GAACAGATAA CTTGTTTTCT 1320 ATTTTCAAAC ATCCACAGAT GGAGAGAAGT TTTGCCCCAA GAGGGACTGT ACCAACAACT 1380 CACCTATATT CAATTTAAAT GATACAGATG ATGAGATTTG GGACTTTAGA GCTGATGAGA 1440 CTTCACTGAC ATTTTGGACT TGAGTTGTTG CTTCAGTGGG TTGAGACATT ATGGGTGAAT 1500 ATATTTTTGC ACTTAGGACA GATGTGAATC TTTGGGAACC AGAGGGCAAA CTAAGTTTGT 1560 GACAACTTGT TACATCAAAA ATAGGAATCT CACACATGGA CCAACAGATA TCAATAGATA 1620 CTTTTCAACC TACAACATCT CATTCCATAT GTTGGCTTTC TTGCCCCCAT ATATTTCTGT 1680 TTTCCTTCCT TCTCTTGAGA CTTCTCAGTC TTTTTTTTTT TTTAATTAAA ATATTTTTAA 1740 ATAATAGAGA TGGGGTCTTA CTATTTTGAC CAGGCTGGTC 1780
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