Tag | Content |
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EnhancerAtlas ID | HS080-18213 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr2:20348310-20349750 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr2:20348426-20348437 | AAACCACAGAA | - | 6.32 | USF1 | MA0093.2 | chr2:20348767-20348778 | GGTCACGTGGT | - | 6.32 | USF2 | MA0526.2 | chr2:20348764-20348780 | CTTGGTCACGTGGTGG | + | 6.05 |
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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 |
GH02I020148 | chr2 | 20348200 | 20349900 |
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Enhancer Sequence | TAGTCTGCTT CTTATTAAAA ACAGACTGGG ACCCAAAGAA ACCCCATCGG GGTAGGTAAT 60 GAAGTAATCA TGATCATACT AAAAGAACAG AATGGAAAAA CTGCCTGGCC TGGAGCAAAC 120 CACAGAAAAA ATTGTCTTCT GCCTCCAGTG CTCAACTGAG CCATTCAGAT GAAAATATCC 180 CACTAGCCAC ATCGACAGCT TAATCTGGGG CAGGGGAGCT AGACATTAGT AAACCGCCAC 240 TCACTGCCCC CTATACAAAT ACATACTTAC AGACACCCAC TCCTACACAC TCAAAATTCG 300 AAGCTCTGGT ATGTGCTCCA TGATTAGGGC TTTCTTTGGG GTTACAAGGA AGCAGAGTTG 360 TAAATCGGTA TTAGAATGTG ATCAAAAGGA ATGTCTGTAT GCAATTATTT TGTTTTGAGA 420 CCAGTGTTCA GAGGCACCGA CTTTAAAGTG CTGGCTTGGT CACGTGGTGG CCTCTCACAC 480 ACATAGGCGC ATATGATTTT GGTCCCCACA AAAGAAGGAA GACAAAGGCC CGGGTTTTCT 540 CTTTGTTGCT TCTTTGTTTC AGGACGGAGT CTCACCCCAA CAGCTCAAAG CACCCTCTCC 600 CCCATCTCCC CTGGCTGTCC ATTCCCTAAC TGTTACAAGA GGAAGTCTTG CTAATATAAC 660 CTCTTGCCCC GGAAAGTAGC AGTTACTGTA ATTTGAGAAC AGAGATCCCT TGCTTAACAG 720 AAATTCACTT AACAAAACTT CAAATTAAAC AAGAGGTCAG TGAAAGGAAA TAACATTTGT 780 GAGGCATGTC TACTGAGTTC TGGGCAGTGT GCTGGGCAAT TTCACACAGA TTTTTGCATT 840 TCATTCAATG AGTCATCACA ACCACCCCAA AGTGGAGGTA TTATTATCCC CCGTATTATA 900 CCAAAGAATC TGAGGCTCAG AGTGGTTATG TAACTTGCAC ACGGTCACAA GGTTAGGAAG 960 TAGCAAACCA AGTAAAAGAT CTCCTCAAAG CAACATCACA GAGAAAAAAA TGTTGAGGAA 1020 TTCGGGTGTC CTATGAGTCC ATCTTGCGGT GGCTGGCTTG CCCAGGCTGC TGCCATCTGT 1080 TACACATGCG CATGAGAAAG CAAAACTCAG TCCATCAGAT AACGTCTGAG AGCAGTCAGT 1140 GCTTTGTGAA GCCCAGCAAG CCACCGTTCA CCAGTGGGCA TAAAACCAAA GCTTTATGTT 1200 TCGGAACAGA ACTGTTAATA CAGACGCATT CTAGTGATTG CATTATCGGC ACCCTAAGTC 1260 ACAAGGCTCT GGTCTGGGTC CCTGTTTACC CAGCTTCATT TGTAGTTGCC TTTCCCTTCC 1320 TCTCTGGGCT CCAGCCAAAT AGCACCTGGC TGTCCCTCGG GGCCACCATG TTCCTTCCTG 1380 TCTCAGACCC TTGGCTATTG CTCTCCCTCT AATTGTCCTT CCCAAGGCAT CTCTTCCCAG 1440
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