| Tag | Content |
|---|
EnhancerAtlas ID | HS093-28615 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr7:76074410-76075620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr7:76074899-76074911 | ATCTGTTTACTT | - | 6.74 | | FOXP2 | MA0593.1 | chr7:76074900-76074911 | TCTGTTTACTT | - | 6.32 | | SPI1 | MA0080.4 | chr7:76075139-76075153 | AGAAAGAGGAAGTG | + | 6.51 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_24594 | chr7:76073995-76074611 | Colon_Crypt_2 | | SE_24594 | chr7:76074734-76075605 | Colon_Crypt_2 | | SE_32292 | chr7:76073902-76075809 | Gastric | | SE_36246 | chr7:76070949-76076101 | HMEC | | SE_50953 | chr7:76073160-76076046 | Sigmoid_Colon | | SE_57688 | chr7:76074718-76075624 | VACO_503 | | SE_58040 | chr7:76074747-76075594 | VACO_9m |
|
| | 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 |
| GH07I076443 | chr7 | 76073119 | 76076316 |
|
Enhancer Sequence | CCCAAGCAGC CACAAACCAC ACCTGGCTTC TTCCTGCCAC TTCTAGCTTA GCAGGTAACT 60
TCATCTGTAA AAAGGGGATG ACGTGATTTC TTGGGGGAAT GAGTAGAGCG CTTGGTAGAA 120
TCATGGCTCA TGCAAGAGGT CTCTGAGCCG GGCGTGGTGG CTCATGTCTG TAATCCCAGC 180
ACTTTGGGAG GCTGAGGTGG GCAGATCACG AGGTCAGGAG TTCGAGACCA GCCTGGCCAA 240
CATAGTGAAA CCCCATCTGT ACTAAAAATA CAAAAATTAG CCAGGCGTGG TGGCATGTGC 300
CTGTAGTCCC AGCTACTTGG GAGGCTGAGG CAGGAGAATC GCTTGAACCC GGGAGGTGGA 360
GGTTGCAGCG AACCAAGATT GCACCACCCC GGGCAACAGT GCGAGACTCC GTTTCAAAAA 420
AAAAAAAAAA AAAGGTCTCT GGCAAAATGC TCCAGGCTTG GGGTCCGACG GGTACTTCTA 480
CCCCTGACAA TCTGTTTACT TATCACCATC CTCTTTTCAG ATGGGGAAGT TCTTTCCATC 540
AGGATTATAG CAAGGATTGG TCTTCATGGC ACACTTGGCA TCCAAGCACG TGTTGTTGGA 600
GCTGTTCTAT GAGCCAGGAG ACATCGGGGA ACGGTTCTTG AAATAAACAT CCGTCTCTTC 660
CTTGTACTCA AGTTCTTAGG GGTTGCAACT TTCTGAGAGC TTGTCCTTCA TTCAACTTCT 720
TTTCTCAGCA GAAAGAGGAA GTGGCTGTGT CAGGGGAGGG GAGGAGTTAT GACTAAGATG 780
TGGCCATGAA TGTCAGCTCC CTGCCAGCTC CAGATGGGCC TCAGCAGGAT AGTTTCCCTG 840
GGCCTTTGCC AGGAGAGACA GCCTCCAGCA GCAATGTCAG AGGGCTCGGC CTGTCTGCCT 900
CCCAGGGGAA CTAGACTGGA AATGAAAGGC AGTGGCAAGC CACTGAGGGT TCTCTAGACT 960
CCATTGCTTA ATCCTCCTCT TTCCCTAAAG TTTCCAGAAG CTTCCTATTG CATTGGAAAG 1020
CCTCTGTAAA CCAACACTTT GGGTGTGGGT TTATTTTTTG AGATGGGGTC TCACTCTGTT 1080
GCCCAGGCTG GATTGCAGTG GCACCACCAT AACTCACTGC AACCTCGACT TCTCTGGTTC 1140
AAACCATCCT CCCACCTCAG CCTCCCAAGT AGCTGGGATT ACAGGGGCAT GCCACCATGC 1200
CCAGCTAATT 1210
|
