Tag | Content |
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EnhancerAtlas ID | HS108-01391 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr1:39297410-39298340 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:39298066-39298084 | TCTTCCTTCCTTCCTGGC | - | 6.8 | EWSR1-FLI1 | MA0149.1 | chr1:39298062-39298080 | TCCTTCTTCCTTCCTTCC | - | 7.2 | HOXA13 | MA0650.2 | chr1:39298166-39298177 | GCCAATAAAAC | + | 6.14 | TEAD1 | MA0090.2 | chr1:39297883-39297893 | CACATTCCAT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGTATCCAAT AAACCCGACT TCAAATTCTA GTAATCACTA TAATCTCTTT TGCCTAAGAA 60 ACATTATTTC TTTCTGGCAT TTTGTAACTG GTCACAAAAA CTGGATCTTT CTGGTTCATT 120 CACCCACTAT CTGCCTGAGC TCATAGCCAA GAATCATGAC CCATACAGTA TGTTAGTGTG 180 TAAGTTAGGG TAACACTAGC TGTTATAATA GATAAAGCCC ATAATCTCAA AAGCTTAACA 240 GCAGAGACAT CTATGTACTG CTCATCAGTC CAATGCAAGT GTTTCTGGTC AGCAGATGAG 300 CCTTCCACTG TGTGATCCAG GAATCCAGAT TCCTTCCGTG TCAAGGCTCT GCATTTTCAA 360 CAGTGTTTCT GTGCTCATCT GCAGTGATCT AGTAGAAGGG AAAAGAACAT GGAGGATCAT 420 GCCTGAGATG ATTACATGGG CTACGCCTAG AAATGGAATA TGTCACCTCC ACTCACATTC 480 CATTGGTAGA ACTCACATAG CCATCCCTAA TTGCAAGAGT GGCTGGAAAT ATTATCTCTA 540 TGCAAAAGGA GAAGAAAGCT TATTCTGCCT CTGCCACAAC GGGTGTGTAC AGCTGCTCTC 600 AGAAAGTCCC GGGATAAGCT GCTCGGAGTC CCAATGTAGC ATTTTCCCTC GTTCCTTCTT 660 CCTTCCTTCC TGGCAGCCTC TAAGAAGCTC TGTTACTATC AGGAAGGCAG ATCTTTGCTC 720 TGGCATCAGA CAGATGGGAC TTCAATTCCA AGCTATGCCA ATAAAACTAG CAATATGTTC 780 CTGCAGGTTC TCTGTGCCTC AGTTTTCTCA TCTGTAAAAT GGACCACAAC AATAGCTCCA 840 ACCTCATTAC ACTGGATGGA TTAGAGGAGA AGGCACAAGT AAGGCTCTTA GCACAACGGC 900 TGGCAAGCTG TAAGCTCTCA AATATTAAGA 930
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