Tag | Content |
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EnhancerAtlas ID | HS108-21638 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:20348470-20349640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
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 | CCATTCAGAT GAAAATATCC CACTAGCCAC ATCGACAGCT TAATCTGGGG CAGGGGAGCT 60 AGACATTAGT AAACCGCCAC TCACTGCCCC CTATACAAAT ACATACTTAC AGACACCCAC 120 TCCTACACAC TCAAAATTCG AAGCTCTGGT ATGTGCTCCA TGATTAGGGC TTTCTTTGGG 180 GTTACAAGGA AGCAGAGTTG TAAATCGGTA TTAGAATGTG ATCAAAAGGA ATGTCTGTAT 240 GCAATTATTT TGTTTTGAGA CCAGTGTTCA GAGGCACCGA CTTTAAAGTG CTGGCTTGGT 300 CACGTGGTGG CCTCTCACAC ACATAGGCGC ATATGATTTT GGTCCCCACA AAAGAAGGAA 360 GACAAAGGCC CGGGTTTTCT CTTTGTTGCT TCTTTGTTTC AGGACGGAGT CTCACCCCAA 420 CAGCTCAAAG CACCCTCTCC CCCATCTCCC CTGGCTGTCC ATTCCCTAAC TGTTACAAGA 480 GGAAGTCTTG CTAATATAAC CTCTTGCCCC GGAAAGTAGC AGTTACTGTA ATTTGAGAAC 540 AGAGATCCCT TGCTTAACAG AAATTCACTT AACAAAACTT CAAATTAAAC AAGAGGTCAG 600 TGAAAGGAAA TAACATTTGT GAGGCATGTC TACTGAGTTC TGGGCAGTGT GCTGGGCAAT 660 TTCACACAGA TTTTTGCATT TCATTCAATG AGTCATCACA ACCACCCCAA AGTGGAGGTA 720 TTATTATCCC CCGTATTATA CCAAAGAATC TGAGGCTCAG AGTGGTTATG TAACTTGCAC 780 ACGGTCACAA GGTTAGGAAG TAGCAAACCA AGTAAAAGAT CTCCTCAAAG CAACATCACA 840 GAGAAAAAAA TGTTGAGGAA TTCGGGTGTC CTATGAGTCC ATCTTGCGGT GGCTGGCTTG 900 CCCAGGCTGC TGCCATCTGT TACACATGCG CATGAGAAAG CAAAACTCAG TCCATCAGAT 960 AACGTCTGAG AGCAGTCAGT GCTTTGTGAA GCCCAGCAAG CCACCGTTCA CCAGTGGGCA 1020 TAAAACCAAA GCTTTATGTT TCGGAACAGA ACTGTTAATA CAGACGCATT CTAGTGATTG 1080 CATTATCGGC ACCCTAAGTC ACAAGGCTCT GGTCTGGGTC CCTGTTTACC CAGCTTCATT 1140 TGTAGTTGCC TTTCCCTTCC TCTCTGGGCT 1170
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