Tag | Content |
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EnhancerAtlas ID | HS060-18614 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:3360070-3361600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:3360984-3361005 | GCGTACTTTCATTTTCAGTAA | + | 6.22 | NFYA | MA0060.3 | chr2:3360730-3360741 | TCTGATTGGTT | - | 6.62 | NFYA | MA0060.3 | chr2:3360801-3360812 | TCTGATTGGTT | - | 6.62 | NFYA | MA0060.3 | chr2:3360814-3360825 | TCTGATTGGTT | - | 6.62 | NFYB | MA0502.1 | chr2:3360731-3360746 | CTGATTGGTTGCTTT | - | 6.7 | NFYB | MA0502.1 | chr2:3360815-3360830 | CTGATTGGTTGCTTT | - | 6.7 |
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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: 2 | ID | Chromosome | Start | End |
GH02I003357 | chr2 | 3359907 | 3360169 | GH02I003356 | chr2 | 3360372 | 3361572 |
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Enhancer Sequence | GCCCCCAGCA ATCTCAGAAG TGGCTGGATT TCCTGAAAGA GAAACGTAGG CTGTATACAA 60 CAGCCTGAAT TGCAATAGCT ATGGTTAATA TGTTTAATAA TTAGAAGATA AAACTAAGAT 120 CTCAGGTGAT GAATCTGAGG CTTAGAGGAA AAAGTTGTAC AACTGGTTAC TAGAGCTGTG 180 ACTAGCACTG CAGGCTTATA AATTCAAATC CATCTGTTTT AGGACAAGCA TTAACTGCAC 240 CTGGATCAAG TTCCCGTGGC CAGCATAATA ATGGCCCTCC ATCCATATCC ACATTCTAAT 300 CCCCAGAACC TGTGAATGTG AACTTACGCG GTAAAGGGAC TCTGCTGATG TGCTTAGATT 360 AAGGACCTTG AGATGAGGAG GCTCTCCTGG ATTATTTAAT CGCATGGGTC ACTGAAATCA 420 GAAAACCTTC CCTGGCTGTA GCCCCAGAGA AATGTGACCA CAGAAAAGAG AATCAGAGAG 480 GTGGTGAGGC AGGAGAACAG GGTCTGGAGG CAGGGCCTAA GGCCAATTCA CCCTGACTTC 540 CTAGAACTAA ACTGAAAGGA AAACGCTAAT TTTCCCCACC CAAGTAACAA AAGGACCAGA 600 GGCTACACCC TTTGCAAACC CTCACCTTTT CTGCATGGCA GTAGGGAAAT TGAAAGTACC 660 TCTGATTGGT TGCTTTTTGC AACTAATCAG ATGTTTGCAT AAAGCTGTAA CTTTGTAACT 720 TCACTGTAGC CTCTGATTGG TTGCTCTGAT TGGTTGCTTT CTACAACCAA TCACACTGAT 780 TGTGGGCCAT CACTTCATTT ACATGGGGTA AACACCAAGT GGCCAATGGG AAACCTCCAG 840 CAGGTATTTG GACCTGAGAA GATTCTGCAT TCAGGGCCCT TGAGCAGCTG CTCGGCCCAA 900 TCCCACCCCA TGGAGCGTAC TTTCATTTTC AGTAACTCTC TGCATTTGTT GCTTCATTCT 960 TTCCTCACTT TGTTTTGTCC AGTTCTTTGC TCAAGATGCC AAGAACCTGG ACACCCTCCA 1020 CCAGTAACAA TGGCAGCTGT GAGGAGGACC CAGTGGCTGT TGCTGGATTT AGAGATGAAT 1080 GAGAGTTGTT AAAGCAAACT AAATATGGCC TGAGAAGGAC TCCCTGCTTC TATATTTGAG 1140 TCCTTGTGGA TGAAACATAA CCTACCTTAA TATGCAGACA AGATTGAGAA CCTAACTTAG 1200 GAGTATGCAC CTGTAACAAC TGAGTCTTGG CCAATCCCAG CAGCCATACT TCAACCACTC 1260 ATACACTGCT GAGTGTTCAA ACTGTGTTCA AATAAGGCAA ATGCCAGCCT GTAACCCATC 1320 CAGCTGTTTC TGCACCTCAC TTCCCATTTC TGTATGTCAC TTCCCTTTAT TTGTTTATAA 1380 ATTTGTCCTG ACCACAAGGC ATCCCTGGAG TCTCTCTGAA TCTGCTGTGA TTCTGGGGGC 1440 TGCCCAATTC ACGAATTGAT CATTGTTCAA TTAAACTCCT TTAAATTTAA TTCAGCTGAA 1500 GTTTTTCTTT TAACAGAGTC CGTGAGCCAA 1530
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