Tag | Content |
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EnhancerAtlas ID | HS104-00709 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:21254150-21255620 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr1:21255067-21255079 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr1:21255067-21255079 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr1:21255066-21255081 | TTCTATTTTTAGTAG | - | 6.57 | PAX6 | MA0069.1 | chr1:21255605-21255619 | TTCATGCATCAGTT | + | 6.22 |
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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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Enhancer Sequence | AAGGAAGAGT TACAGAGGGT GGCTGAACTG GGCCAAAAAC ATAAGGGACC AAGTTACAAA 60 CAAAGAAACA GCAGAATCAC TACTTCCAAA ACACAGATCC CTTATGTTCT GATCATGAAG 120 AACCACTCTG CTTTGCCGGC CCAACTGGAT ATTTCATATC TGTGACATCG AGCAATGCCT 180 CTAGAATGAT TGCTACAGGT GTTTTTTGTT TTGTTTTTTT GACAGGGTCT TACTCTGTCA 240 CCCAGGCTGG AGAGCAGTGG TGTGAACATG GCTCAGTGCG GCCTCAATCT CAAAGGCTCA 300 AGCAATCCTC CCATCTCAGT CTCCAGAGTA GCTGGGACTA CAAGCACACA CCACCATGCT 360 TGGCTAATTT TTTATTTTTT TGTAGGGACG AAAGGTCTCC ATATGTTGCC CAGGCTGGTC 420 TTGAACTCTA CAGGTGGTAC ATTCAATACC AAGCTGAGAA CACCCTCTCA AACTGAGGTA 480 AAATTTAACT AGTAGTAAAG TAATAAGACA GAATAAAAAC AATACAGTTT TTATGTATAC 540 ACTATATAAG TAATTGTTGT ATAAATTTAT TTATACAACA ATAGCATGTG TCAAAAGATG 600 ATATAATTTT TGGCTGTACA CAAATACTCC TGTATCTCCG ATACTGTCAA TTGTGGTGTT 660 CTTGTTGAAA TTTACTTCCT CAATTTCTAA GCTATAACTT CCCTAAGCAA ATCCTTATAT 720 AGATGCTGGT GGCACCACCA TATCATACTC ATTTTTCTTT TATTTGAGAC AGTCTCACTC 780 TGTTGTCCAA GCTGGAGTGC AGTGGTGTGA TCTCGGCTCA CTGCAACCTC CGCCTTCCGA 840 GTTCAAGAGA TTCTCCTGTC TCAGCCTCCT GAGTAGCTGG GACTATAGGC GTGCACCACC 900 ATGCCTGGCT ATTTTTTTCT ATTTTTAGTA GAGACAGGTT TCACCATGTT GGCCAGGATG 960 GTCTTGATCT CCTGACCTCG TGATCCGCCC CTCGGCCTCC CAAAGTGCTG GGATTACAGA 1020 TGTGAGCCAC CACGCCAGGC CCCTCTTTTT AAAATATATA TGTAATATTT GTTGACATAT 1080 AATTTACGTA TCATAAAATT AACCTTTTAA AACTATACAA TTTAATGGTC TGTGGTATAA 1140 CCACAGTTGT GTGACCACTA CCACTATATA ACTTTAGAAT ATTTTCATCA CCCCAGAAAG 1200 AAGCTCGGTA TGTATTAGCA CCGTCTCCCC ACTCTCTTCT CTCCCCAACC CCTGGTGAGC 1260 ACTAATTTAT TTTCTGCTTC TATGGATTTG CCTATTCCTG ACATTTCATA CAAATGGAAT 1320 CATATAAAAT GTGGTCTTTT GTGACTTTTT TCACTTAGCG TAATGTTTTT AAGGTTCATC 1380 CATTGTACAC CATGTGAATT TCATTCCTTA TCATGGTCCG ATATTTCATG GTATGTATAT 1440 ATCACATTTT GTTTATTCAT GCATCAGTTG 1470
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