Tag | Content |
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EnhancerAtlas ID | HS104-17966 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr13:114206850-114208470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAX | MA0058.3 | chr13:114207200-114207210 | ACCACGTGCT | + | 6.02 | NR2F1 | MA0017.2 | chr13:114208316-114208329 | CCTGTGACCTCTG | - | 6.19 |
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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 |
GH13I113553 | chr13 | 114207501 | 114207650 |
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Enhancer Sequence | TTATAAACAG GATACTTAAA GGTTCTTGGG ATATTGAACA ATGAAAGAAA TTGTACTATT 60 TGAAAATTCT ATTTCACATG AAAATGTAAA ATTTCAGCAT ATCAGAAAGC ATCGTGAACA 120 AATTTGAAAG CCAAGCAAAA CTGGGAAAAA TATTTGGATA AAAAAATCCT AACACTGGTA 180 CATAATACAT AATAGGCAGT TCATATGTAT TTTTTGTATG AATGAAACTT ACAATACTTT 240 TATTAATGTC ATGGGAACTT ATAAAAACTG CATGGAGATA TTTTAAAGAA AAAATTTTGA 300 AACCCATTTT GGTTTTCTTT ATAATTCCTT CAGTTCAGCC CATTCCTGTA ACCACGTGCT 360 CATCCCCACA GGACTAGGCA GTGCCCACCC TTGGTGCCCT GCAGTGCACC GCAAGGACAT 420 GGCCGTGGCC TGGAGCCGCG TCCCTGAGTT CCTGGTGGGC CGCGTGAGTC TCCCTGTTCC 480 TCCCTGCTGC CTTCTCCTCT CCTGGCTTCC CCACCCCATA CTTCCCTGAT GATATGGTTT 540 GGCTGTGTCC CCACCCAAAT CTCATTTTGA ATTGTAATCG TCATGGGTTG ACCGAGGGAG 600 GTGATTGGAT CATGGGGGCA GATGTCCCCC AGGCTGTTCT CATGATAGTG AGTTCTCACA 660 AGGTCTGACG GTTTTAAAAG TGGCAGTTTG TTCTCGCGCT CTCGCTTCTC CATCCTGCTG 720 CCTTGTGAAT AAGGATGTGT CTGCTTCCCC TTCTGCCGTG ATTGTGTTTC CTGAGGTCTC 780 CCCAGCCATG GAGAACTGCA AGTCAATTAA ACCTGTTTCC TTTATAAATT ACCCAGTCTT 840 GGGGAAGGCG TGAGAACAGA CAAACATGCC TGAGTCCCCG AGTCTGTGAT GCTCCTCATT 900 CTTCAGCACG GCCTGTGCCC GGGACGGGGC GCTCCTCCAG TGCAGAGCTC ACACCATGAC 960 TGTGGTGTCC TTCAAATAAC ACTGCTGCTG CCAGCTTCCC AGGGACTCTT CTCCTGTGTG 1020 ATTCCAGTGC CTTGCCTATG TCCCTGCTAA TCTTCTGGAG TTTAGGGGTC CGTGCGAAGC 1080 CCACCCCACC TGAGTCCTTT CATCCTGGGT GCCTTCACCT CCGTCCAGGA CTCCGGGGTT 1140 GCAGCCACAC ATGCTCATGT CACCGTGAGG CCCAGCCCTC CAGGGCCTGA GATGTACAGA 1200 TGCTATCCCC CTGGGCACCC AGTGTTTCCC CTTCCTCCCT GTCTGCCTTT TGCTCAATCT 1260 CTCAGCGCCC TCAGGAAGCC CTTTCACAGC TCAGCAGGGA AACCTCTGGG CTCCTCCCCC 1320 TCCAGCAAGT CACCTGGAAG CTCTCAGGCT GGCCATGGAA AGCTGAACCC ACTGCCAGGG 1380 GACTGGACAG AGAGGCTGGT CTCATTTTCC AATCCCTTCC AGAAGGAAGG AGGATGCTTC 1440 TCCTGAGAGC AGCGACAGGT TTGTGTCCTG TGACCTCTGC CTTCCCTCGC CCGGGGGAGG 1500 GTGATGGGGC GTCTTTTTGG CTTTGGTTTA AGTAGCAAAA GAGATGGAGT GTTCAAAGGA 1560 TTGAGGGGTC GGCCGAGGGT GGGGCTTCTC AGTGAGGGGC GGGTCCTCTG GGCGTCATGA 1620
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