Tag | Content |
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EnhancerAtlas ID | HS108-04798 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr10:5870520-5872000 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr10:5871189-5871200 | TTAATTAAATT | - | 6.32 | PHOX2A | MA0713.1 | chr10:5871190-5871201 | TAATTAAATTA | - | 6.62 | PROP1 | MA0715.1 | chr10:5871190-5871201 | TAATTAAATTA | + | 6.32 | PROP1 | MA0715.1 | chr10:5871190-5871201 | TAATTAAATTA | - | 6.62 | Phox2b | MA0681.1 | chr10:5871190-5871201 | TAATTAAATTA | - | 6.62 |
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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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Enhancer Sequence | AGAGTAAAAC TTTGTCTCAA ACCAAAAAAA AAAGTTAAAA AAAAACAATT AAATAAGAAA 60 GTCCCTGGAT CCAAGGACTC CAGCACAGAG AACGAACCTG GCCCATAGAA ACTGAGATGG 120 AGGACGGTGA AAGGCACTGT GCGGACCTCC CTGGCTGCAG GAGCTCTGAG CACGTCCGCG 180 ATCCTGGGAG TGAAAAGGCC TCCCTGGCTG CTCTGACTTG CTATGGTCAG AGGGGCACAC 240 CTGGCTTCTC AAGCAAGCGT ATCTAAAAGC AAGAGACCTC CTCTCTTCCA TGAAAATGAA 300 AGCACCTTCC AGACAGGGAC TGACCCGGGC CTGTGTTAGT TTGAAAGACG TGCTTCAAAG 360 CCTGTTGCGT TAACCTGTGG ACCTACGCTG TGGCCCTTCT ACTCGCCGTT CTTCCAACGC 420 AGATGAGCCC ACCCTCGTGT TTCTGTGCTG TCATGAGACG GACAGTCTTC CCGTCACAGT 480 TGCAGTGCTG GCTTGTCGAG TTGCTGTTCC TAGTTCACCT CTGCAACTCC AAATCGTCAA 540 ACAATTTAGA ACCACTAGAC TCTAGAAAGA GACCAGAAAG CACTTTTGAG ATCCCATTTA 600 ATCTCTCCAC TAGGAAACCT ATAGCTAAAG AAGTTTACAT AACTTGTCTC CTAAACTGTC 660 ATCTCTTGGT TAATTAAATT AAATTTCTCT TCCGGTGGGA TCCTGTCAAC TTTGTGTTTT 720 CGTGAAGCCT TGCTTTATGT TTTGAAGGTT GAAAGTTAGA CCCAGAGAAT TTCTTCAACA 780 TTCAGTCCTA TGACTTCCGA GCCACTATTC ACACAGAAAA GCTGTCAGTG GGCTTTATCT 840 TTGTTTTGCA GGAGACCAAA CTGATAGGTT GGCCCGACTA GCTTGTGTGC TTTACTTGTT 900 ATCTTATTTG TTGGCACAGC AAGAAAACAG CCAATGGCCA GGCATGGTGG TTCATGCCTG 960 TAAGTCCAGC ACTTTGGGAA GCCAAGGCGG GCGGATCACC TGAAGTCAGG AGTTCAAGAC 1020 GAGCCTGTCC AGCATGGTGA AACCCTGTCT CTACTAAAAA TACAAAAATC AGCCAGGCGT 1080 AGTGGTGCGC GCCTGTAGTC CCAGCCACTC AGGAGACTGA GGTACGGAGA ATCACTTGGA 1140 TGCAGGAGGT AGAAGTTGCA GTGAGCCGAG ATCGCACCAC TGCACTCCAG CCTGGGCAGC 1200 AAAAAAAGAA AACAGCCAAA ATACAAGTTA AATATATGCA CTGACTCTGT ATGCTTGATG 1260 CCTATAGCTT TTCTGTATAG CATTCTTTTA TTATTTTAAG CAAAACTTTA TTTTTCACAT 1320 AAGCATTTAG GCAGCAGTAA CTGATAGGAG CAGATGGCTG GGAGATTAAA AGATAGGTCA 1380 GTGGGCCACT CAGTTTGTCC TGGAATTATT AAGACAAATC CTGTTTCCTC TCCTCATCTG 1440 TTTCCCACAC TTTCTCTTGT TCTCCTCCTT TCCTATTTCA 1480
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