Tag | Content |
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EnhancerAtlas ID | HS104-05724 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:224564720-224566110 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr1:224565766-224565776 | TTTAATTAGA | - | 6.02 | FOSL1 | MA0477.1 | chr1:224565544-224565555 | AGTGACTCATG | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 224564756 | 224565006 | chr1 | 224565452 | 224565753 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I224376 | chr1 | 224564092 | 224568999 |
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Enhancer Sequence | GTACCCAAAA GATTAAATGT TACATGTCCT TTTAGTCCTT GACCAGGTCT AGCCTTGGCA 60 GAAGCAAGGG AGCCACTAAG CCAAACTCCC TGTGCAGACA GACCATGTTT CAAGGCTGGA 120 AGTAGTGCCC TGGCAACACA CAAAAGGAAC GGTGAAATGG TAGGCAAAGT GAACTTGGCT 180 CTGCTGGCCT CTTTGGGGTC ACAGAAATTG CTCCTTGTGG TAATCTTATA TTTCTGTCAG 240 GCACAGGGCC AAGAAGCTGT GTAACAGACA TTACTTTGCT TGCATCTCTT TTTCATACCT 300 TTTCCCTCTG AGGCAGCTTT TGCTTAGAAA ACAGTCCCTT CACTCTGCCT TTCCTCCTAA 360 CTTCCTGTGC CTCTTCATGT TCTGCTCAAG CTTTTTAAAG CAACGAAGCT GTTGGAGAAC 420 TTAAATCCTT GCAACTGAGA GATAAGCTAC TTAAAGGCGG TAGAGATCTT TTTTTTTTTT 480 TTTTTGAGAT GGGGTCTTGC TGTGTTGCCC AGGCTGGAGT GCAGTGGTGT GATCTCAGCT 540 CACTGCAACC TCTGCTTTCT GGGTTCAAGC GATTCTCCTG CCTCAGCCTC CCAAGTAGCT 600 GGGATTACGG CTAGCTACTC CTGGCTAATT TTTGTATTTT TAGTAGAGAT GGGGTTTCAC 660 CATGTTGGCC AGGCTGGTCT CAAACTCCTG ACCTCAAACG ATCTGCCTGC CTTGGTCTCC 720 CAAAGTGCTG GGATTATAGG TGTGAGCCAC TGCGCCTGGC CATGTAGATG ACTTTTGACC 780 AAAATGTTTC ACCTTCTCAT TCAGATATTC TTAGTAACCA AAACAGTGAC TCATGCAGTT 840 GAGAGAGCCT TTGGGCTGTC AGTTTACAGT ACATCAGGCT TGCTGAGGCT AAGCAAATCA 900 GAAAGGTGCC ATGTTTATAA CAGAGGTCAA AGCTCCTTAC TTCTGAAACA TTAGCTGTGG 960 TTAAAAACAA AAACTCTTCC TTCTTGTATT GCTTGTCTAT CAAAGCCAGG AAAGTGGGGG 1020 ATCACTGTAG TTAAATTTTT TTTTTTTTTA ATTAGAGACA GAGTCTTGCC CTGTCGCCCA 1080 AGCTGGAGTG CACTGGCGCA ATCGTGGTAC ACTGCAGCCT TGAACTCCTG GACTCAAGCA 1140 GTCCTCCTGC CTCAGCTTCC CAAGTAGTTG GGAGTAGGTG CACACCACCA TGCCCAGCGA 1200 ATTTTTTGTA GAGACAGAGG TCTTGCTATG TTGCCTAGGC TGGTATCAAA ATTACTGGCC 1260 TCAAGCGATT CTCCTGCCTC GGCCTCCCAG ATGTTGGGAT TACTGGTGTG AGCCACCACG 1320 CCCAGCTCAA AAACAATTTT TTTAGGGGCA CTTCTACAAA TCATGAAAGG GGGATAAAAG 1380 CACTGACTTT 1390
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