| Tag | Content |
|---|
EnhancerAtlas ID | HS176-37468 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:76074730-76075730 |
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 | | Nr2f6(var.2) | MA0728.1 | chr7:76075674-76075689 | TGAACTCCTGACCTC | - | 6.22 | | SPI1 | MA0080.4 | chr7:76075139-76075153 | AGAAAGAGGAAGTG | + | 6.51 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| 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 | GAGGCTGAGG CAGGAGAATC GCTTGAACCC GGGAGGTGGA GGTTGCAGCG AACCAAGATT 60
GCACCACCCC GGGCAACAGT GCGAGACTCC GTTTCAAAAA AAAAAAAAAA AAAGGTCTCT 120
GGCAAAATGC TCCAGGCTTG GGGTCCGACG GGTACTTCTA CCCCTGACAA TCTGTTTACT 180
TATCACCATC CTCTTTTCAG ATGGGGAAGT TCTTTCCATC AGGATTATAG CAAGGATTGG 240
TCTTCATGGC ACACTTGGCA TCCAAGCACG TGTTGTTGGA GCTGTTCTAT GAGCCAGGAG 300
ACATCGGGGA ACGGTTCTTG AAATAAACAT CCGTCTCTTC CTTGTACTCA AGTTCTTAGG 360
GGTTGCAACT TTCTGAGAGC TTGTCCTTCA TTCAACTTCT TTTCTCAGCA GAAAGAGGAA 420
GTGGCTGTGT CAGGGGAGGG GAGGAGTTAT GACTAAGATG TGGCCATGAA TGTCAGCTCC 480
CTGCCAGCTC CAGATGGGCC TCAGCAGGAT AGTTTCCCTG GGCCTTTGCC AGGAGAGACA 540
GCCTCCAGCA GCAATGTCAG AGGGCTCGGC CTGTCTGCCT CCCAGGGGAA CTAGACTGGA 600
AATGAAAGGC AGTGGCAAGC CACTGAGGGT TCTCTAGACT CCATTGCTTA ATCCTCCTCT 660
TTCCCTAAAG TTTCCAGAAG CTTCCTATTG CATTGGAAAG CCTCTGTAAA CCAACACTTT 720
GGGTGTGGGT TTATTTTTTG AGATGGGGTC TCACTCTGTT GCCCAGGCTG GATTGCAGTG 780
GCACCACCAT AACTCACTGC AACCTCGACT TCTCTGGTTC AAACCATCCT CCCACCTCAG 840
CCTCCCAAGT AGCTGGGATT ACAGGGGCAT GCCACCATGC CCAGCTAATT TTATTTTATT 900
TTTTTAGTAC AGACGGGGTT TCACCATGTT GGCCAGGCTG GTCTTGAACT CCTGACCTCA 960
AGTGCTCCTC CTGCCTCGGC CTACCAAAAT GTTGGGATTA 1000
|
