| Tag | Content |
|---|
EnhancerAtlas ID | HS108-31358 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr4:183858950-183859820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr4:183859434-183859453 | TGGACTCCAGGGGGCAGCA | + | 6.24 | | Lhx3 | MA0135.1 | chr4:183859795-183859808 | AGTTAATTAATTA | - | 6.64 | | Lhx3 | MA0135.1 | chr4:183859798-183859811 | TAATTAATTAATT | + | 6.78 | | Lhx3 | MA0135.1 | chr4:183859799-183859812 | AATTAATTAATTT | - | 6.92 | | POU6F1 | MA0628.1 | chr4:183859800-183859810 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr4:183859800-183859810 | ATTAATTAAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I182938 | chr4 | 183859361 | 183859510 |
|
Enhancer Sequence | AGACAGATGA GAAAAAGAGA ACAGAGAATG AAAGAGCTCA AAGCAGCCCT GTATTAGTTT 60
GCTGGGGTTA CCATAACAAA ATACTACAGA CCAGTGGCTT CAACAACAGA CGTATTTTCT 120
CACAGTTCTG GAGGCTGGAA GTCCAAGATC AAGGTGTCGG CAGGGTTGGT TTCTCCTGGG 180
GTCTCTCTGC CTGCCTTGCA GACAGACAGC TGCCTGCCTT GCAGACAGAC AGCTGCCTTC 240
CCTCCCTGTC CTGACCAGGT CTCTGTTGTT TGTCTTAATT TCTTCTTTTA AGGAAACCTG 300
TCATATTAGA TTAAGTCCTA ACCATAAGAC CTTCTTCTAC CTTAATTACC TCTTTAGAGG 360
CCCTATCCCC AAATACAGTT CCATTAGAGG TTAGGGCTTC AACATGTGAA TTTTGGCGGA 420
AGGGGACACA ACTCGGTCCT TGACAGGACT CAGACTTCAA GGACACTCAG GGTTGTGCTC 480
AGCGTGGACT CCAGGGGGCA GCAGAGATTT GCAGCCGGCC TGGGCAGAGG GCAAGGCCAC 540
ACTCCAGGCC CGCTGTCGCG TGCCCTCGCC CTCAACGTTC CCTCTCGGAT TTTCAGGAAT 600
TTCATTTCAC GTCCTTGTTC CCTCCTATGT AACTGACAAC GCAGAATCCG CAGGATGTGA 660
GGAGTGGACC CCTTATTAAC TCCAGTTCCC AAAATCACAA AAATATGGAA CCAAAATGAG 720
CTGCAATTGA CAAAGCAGGA TATTATACAG AGAAAACTCC TGAAAGCATG GCTAGAGATA 780
AAGTAGCTGA GGTCTATATA ACTTGCTCGT AAATTAAGGT GTTTTTAACA TTTTAAAATT 840
AATTTAGTTA ATTAATTAAT TTATTATTAT 870
|
