Tag | Content |
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EnhancerAtlas ID | HS104-54243 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr7:29217440-29218560 |
Target genes | |
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) |
Lhx3 | MA0135.1 | chr7:29218350-29218363 | CATTAATTAATTA | - | 6.46 | Lhx3 | MA0135.1 | chr7:29218353-29218366 | TAATTAATTAATT | + | 6.78 | Lhx3 | MA0135.1 | chr7:29218354-29218367 | AATTAATTAATTT | - | 6.92 | POU6F1 | MA0628.1 | chr7:29218351-29218361 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr7:29218355-29218365 | ATTAATTAAT | + | 6.02 | POU6F1 | MA0628.1 | chr7:29218351-29218361 | ATTAATTAAT | - | 6.02 | POU6F1 | MA0628.1 | chr7:29218355-29218365 | ATTAATTAAT | - | 6.02 | TEAD1 | MA0090.2 | chr7:29217669-29217679 | CACATTCCAT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 29217551 | 29218329 | chr7 | 29217860 | 29218383 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I029177 | chr7 | 29217470 | 29218610 |
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Enhancer Sequence | ATCTTTTTTT CCAACCCAGA CCTCTCTCCA AACCTTGCTA CTTGACATCT CCTTAGACAT 60 TTCATAGGTG CCTCAAACTT CACATGTCCG AAACACAACC CTCGGTTCCA TCCCCACACA 120 AAGTTCCCCC TCCCCAAGCC CTCACCATCA CAGCAAGTGG CACCACCAGC CATTTAACTG 180 CTCAGCTAAA AACCTAGGAG TCACCTTGAT GATTGTTTAT CTCATGCCTC ACATTCCATC 240 ATCAGCAAGT GTTGTCAGAT TCTACCCTAA GTCTGATGGT GTCTTGCCAT CTCCACTGCT 300 ACTATCCTCT GTCCACACCA TCAGCCTTTC TTTGAAACCA CTGGAATAGT CACATAGCCA 360 CCGTGCACCC TGCTCTTCTT ACTATCCTTT TCCATAGCTG CCAAAGTGAT CTTTTCAGTA 420 TGAATCAGAA CATGTTATCC CCTTCCTAAA AGCTTCTGTG GCTTCCCATT GTGTCTAGAA 480 ATAAACAGAA AGTCTCCACT ATGACCCACG TGGCTGCTAG GATCTGACAT CTACTCAGCC 540 TCTGACCTGG TCTTCCTCTG CGTGCGGTTT CATTCCTTTG ACGCCAGCTC CACTGGCCGC 600 CTTTCCTGTT CCTCTAACAT GCCCAGCTCG TGTCTGACTC AGCCCTTTAA ATCTGCTGTT 660 CCCTCCTCCA GACCTGCAAG ATCAAGTCTC TGCTGAAATG TCACATCCTC CGAGAGACGT 720 TGCCTGACAT GCTGTTTTAT GTTCATCTGA ACACATTTTT CAGCATTTGA AGTTATCTTT 780 TTAAAAAAAG CAGTTCATTG TCTGTGCCTC TTAAGGGCAG GGACTTTGTT TATTGTTATA 840 TTCTCAGGGT CTATACCTAT GCCTGGATCA TAGTAGGGGC TCAGTTATTG TTTGTTGAAT 900 GACTGTTTGG CATTAATTAA TTAATTTCAC AACTTGGAGT GGAATTAGCC ATCTGCATTC 960 ATATGAAAAA TGACTTAAAT CCCTATGATA TATCAAATTA AGGCAAATAA TCAGCCAATA 1020 AAAATGGGTT TGCCACAAAT TTGACCAATC AAAGGTTAAC TACTATGTAA AGAGTTATTA 1080 CAAACTAATA AAAAGAACAC TAACACACCA TTTAAGGGAC 1120
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