Tag | Content |
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EnhancerAtlas ID | HS080-02359 | Organism | Homo sapiens | Tissue/cell | H9 | Coordinate | chr1:162061300-162062710 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Pou2f3 | MA0627.1 | chr1:162062399-162062415 | TCAAATTTGCATACCC | - | 6.35 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 162061529 | 162061677 | chr1 | 162061754 | 162062275 |
| | Number: 1 | ID | Chromosome | Start | End |
GH01I162091 | chr1 | 162060892 | 162063064 |
| Enhancer Sequence | AAGACTCAAT AAATATATTG CCACCATTTT CCCAGAATTG GGATATTGCT TTTAATTTTC 60 ACTACAGTGT GGCAAGTTGC TGACTGAGAT TTTAAGTTAT TTTTCCCCCA TGGAGCAGCA 120 AAACATATAA AGATTTGAGA ACATAGGATA AGGAATGAAT AAATCCTGCT TATGTGTAAT 180 TACATTTGAG CAACATGTTG ATGAACAGCT AAGGGAAGAC AGAGATCACA AGTTTCCTCC 240 TCCCACTCCT CAAAGAGAGA GGGCACTTTA CACAGCCCAG GAGCATGTGG AGTGCTGTGC 300 AGTCTTGCTG TGTTCTGGCT GTTTGCTCTA ATTGATCTGT CAACCACTAC GTGGGCATTA 360 AGTAATTGGG ATGTGACTTC ACTGGGGCAA GGTGGGGTGG TCTGCAGAAT ATACAGGAAG 420 AATCAAATAT AGAATCACGG AGTGCTGGAG TTGGAAGGGA CCTCAGAGAT CACCTCTGAG 480 ATTAGGTCCT AAATCAGCTC TGTTATTTTG CAGATGAGGG GGACTGAAGT ACAAAGAGAT 540 GAAAGTGACT AGTTCAAGGC TGTGGATCCA ACAAAGGATG GGATTGGCAT TGCAGCTTGT 600 CCTGAACTCT CCCAGGCCAC ATTCCAGTCT CTCAAACCCC AGCTTCCCTG TTGAGTAATG 660 AGTAAACAGA CTATTGTAAA ACGAAGAGGA CTTTTATAGA GTAAATTGAA GGGTATTCAT 720 TCATTCTTTT GTTTTAGGAA GTTCAGTGTT TCAGCTAGTG GATTTTCTTA AGATACAGGC 780 ATGCAGAATT TGGTGTTTGT GTGGAATAAT TGAGGGAGAG AACAGAGGAG GATTTCATCA 840 GCACTATCAC AGCTCTCCTG TGGCAGAATC AAGAGCACAA CCAGAAGGCC TGGCTTCGTC 900 AGTCCTGTTG AACTTTTCAT GCCACCAAGT GGTAAATCTG GTGATTGTTG ACATTTCCAA 960 GAAAAGTGTT TCTCTGAAGG CTCCATGCTA TTCACTGAAT AAGAGTTTAT GACTGACTTA 1020 ATGAATTGAC ATTTTATTTA TCTCAGTGCT TATTCTCTCT CAGTGGTCTT TTTGTTTCTT 1080 TGGGCAAGAA GATAGTAATT CAAATTTGCA TACCCTTGCC TGGTACATGA TTTATGCTCA 1140 ATGTATATGC AGTGAATGAA TCTGTTTGGA GAAATGGGAC TAACATGTGA AAAGATGAAC 1200 AAACTCACCT ACTGTGTGTT GTTGAGTACT AAATTATATG CCACAGATCC TGAGAAGAAG 1260 ATGCAGTGTG GGGAGGCTTC CTGATGAAAT GGTAAGGAGG ATTTACTCCT CCTGCATTCA 1320 CCAGGCCAAG CCCTTATTCT TCTTTAGTAC CATAAATGAG GGGATACGAG AAAAATGGCT 1380 CCTTTAAGCG GCAAGTGTTT GGCTGCTTCT 1410
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