Tag | Content |
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EnhancerAtlas ID | HS104-02770 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:86895040-86896540 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr1:86896498-86896509 | TGCTGAGATTT | - | 6.32 | ZNF263 | MA0528.1 | chr1:86896396-86896417 | AGAGGAAAAGGGGAGAGAGGG | + | 6.05 | ZNF263 | MA0528.1 | chr1:86896028-86896049 | TTTTTTGCTCCTTCCTCCTTC | - | 6.16 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 86895065 | 86895376 | chr1 | 86895452 | 86896393 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I086428 | chr1 | 86894502 | 86896754 |
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Enhancer Sequence | AGAGGTCTGA ACTGCTGCAG AAGGAAAGGC AAGAGGCACG TGGAGACAGC ATTAAGGAAC 60 AAGGCACACA CCAGGTTTTT GTCAGACATG GAAAAAACCA GCTTCAAGAA GAAATCCCAC 120 AAGTCTGGAT CTAGGCAAAT TCATTGTGAA GAGCAATAGA CTATGCCAGG GAAAGTGGTT 180 CAGCCTGTGG TTAGATATTG ATGGCTGGAG TTTGGGAGAG AAGTCAGGGT CATAGGCCTA 240 GAGACTGGTA TTTAGTGAGT GAGATCTGAG GGAGAAAATA GTAAGCACAG TTCGCCAGTC 300 AAGGACTATC TATCCCAATC TTTATTTTTT GTTTTTGATT TAATGTAACA GTAGTGCCTT 360 TCAAGTGATG TCTTAATTTT CTTTTTTATC CCTAGTTAAA TCTAAACTAG GGTTTTGTTA 420 ACAAGGATTT TGTTATCCTC TGTATAGTTA GCAGGAAGTG GAGTGAAACA CTCCATAAAA 480 TACACTTTAC AAAACACTTT ATAAATCTTT AGAAAAACGT AGTTTTTTTT CTTTCCTGGT 540 AACCTTGAGA TGCTGATAAT CTCTGCTCAA GCATGATTTC ATCAGCACTT CTAAATTTCA 600 TGAGTAGGCA CAATCTTTCC CTCAACACTC ACAGCTTGGA CTGCTACCCT CCCTTCCTTT 660 GCCTCGAGGT CCAAAAATTA CACAATATGC CACAGCCTGA GTCAACTCAG CACACACTTC 720 CTGAGTTCCC GGAACTTAAA ATAATTCAGA AAAAAGAAAT GTGTGCTTTG GGAGGGGAGT 780 TCATCTGGAA AGCTTATATG GGAAAGCTGT GGTCTGAACT TTGAAGGGAA TGTAAGATTT 840 TGAGAGAGAG GAAGTTCTAA AGGATCTCAT GCAGAGGATG GGGGTTTCCC TGACCTAGGA 900 GCTGTAAAAT ACACATAAAC ATGGAGAATA AGGGATAAAA TAAAAGAGAA GGGACCATCC 960 AGGCTGGGGA GAACATTCTG CAGTCTCCTT TTTTGCTCCT TCCTCCTTCC CTAGCTCCTA 1020 GGTTTCAACT ATTGCTCTAG ATAGAAGAAT TACCTGCAAG AAAAAAAGCA GGTCTGCTTG 1080 GATAGCTCAG ACAGAAGATT AGGAAAGCTT TATTTGCCTA TCTGGATATG CTTCTTTCCC 1140 TTTCTCCAAA CCCTGAACTT AGAGGCCTCT ACAAAGCTGA ATAGAAACCT GTTGGGCAGC 1200 TTCACTGGGG AGATGAGAGG ATGTGGGACT ACTCACTAGC TTCAAATAGA TGTGCAACAA 1260 GTAAATTACT GCATTTACAA GACCAAACAT ATTTTCATGC TGCCTTTTTT ATGGTGGTAG 1320 GTGGTGGAGT AGGAGGAGAT GGGAATAGGA TAGGGGAGAG GAAAAGGGGA GAGAGGGAAG 1380 TAACTTAAAC TCTTTGGTCA TTCCAAAGAG TATGTGTGGT CAAGAAATGT TACGTCTTCA 1440 CTAGTTAGCA AGGCACATTG CTGAGATTTT AGAAGCTCAA AAGCAAAAGT TCTTTCTTCC 1500
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