Tag | Content |
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EnhancerAtlas ID | HS060-19047 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:39703520-39704690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr2:39703838-39703859 | AACTGCTTTCACTTTTTCTTC | + | 7.27 | SPIC | MA0687.1 | chr2:39703853-39703867 | TTCTTCCCCTTTTG | - | 6.21 |
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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 |
GH02I039476 | chr2 | 39703261 | 39704473 |
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Enhancer Sequence | AATCTATTAT CACTATCATT TTGGATTGGC GTGGTCCTCA AAGCCCCATC TTGACTAGAA 60 ATCAACTAGC ATTTGCTTCT CTGCAGTTCG TAATCTAGCT TCCTCTCTCA CCTTTCTCTT 120 GGCAATTGCC CTCTCTGAAG TCACTGCTGT TGTTTCCGAG TCACTGAATG AAACCGTTTT 180 TCCTTCAGCC CCCATTTTCC TTCACTCCTC TGCAGCATCC AGCAGTGTTG ACTGCTCTTC 240 CTTTTACCTC TCTCCTGTTG GCTGTTAGGA TGCTCTGCTG TCCCGGATCA CTACCTCTTC 300 TGATGCTTCC AGTTTTTAAA CTGCTTTCAC TTTTTCTTCC CCTTTTGTAA CTGTGGATGT 360 CCCACAAGGC CAAGTCCTTG GTGCTCTGGT TTTACCCTCT ATTTCAGCTA ATTTTGCTTA 420 TTCTCATCTT TGGTCATTGC TAAGTCCCTA TCTGTTCACC AGGGCTTCCC CCTCCCCTGA 480 GTTCTAAGCT ACAGATCTGC TTGTGACACG TTCCACTTGA TGCCCTGCTG TTCCATCAAA 540 TTTCCTCCCC TTTAATCCTC CCAAATGCCA TTACAGATAT CATTATTCTT AGATGGAGTC 600 TTGCTCCGTT GCCCAGGCTG GAGTATAGTG GTGTGATCTC GGCTCACTGC AACCTTCACC 660 TCCTGTGTTC AAGTGATTCT CCTGCTTCAG CCTCCTGAGT AGCTGGGATT ACAGGCATGC 720 ACCACCACAC CAGAGTAATT TTTGTATTTT TTGTGGAGAT GGGGTTTCAC CATGTTGGCC 780 AGGCTGGTCT CAAACTCCTG ACCTCAAGTG ATCCTCCCAC CTCAGCCTCC CAAAGTGCTG 840 TGATTACAGA AGTGAGCCAC CATGCCCAGC CTGTTATAGA TATCATCTTT CCCTTAGTTT 900 CTAAGGCTCA GAATCATACC CTTCCTTGAT TCCTCATATT TTCTCCAGAG TCAGTTAATT 960 ATACATCCTA TCCATCCTCT TTCCTGTCAT TTCCTCTTTT TGCCATTGCA CGGCTCACAC 1020 ACCTGCTATG GTCCCTTGTT ATTTCTTCTT TTGGACCATT TTGGTATTCT TCCAGAGAAG 1080 CAGGACAGTT AAATGTGGCA ATATTTGGAC TCATTTGTGT TCAAAATTTG TGATATGGAT 1140 TCTTCCCACA TCCCCTGCCC CAATAACAAA 1170
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