| Tag | Content |
|---|
EnhancerAtlas ID | HS069-00042 |
Organism | Homo sapiens |
Tissue/cell | GM18951 |
Coordinate | chr1:9170410-9171330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:9170986-9171005 | CGTCCACCAGGGGGCAGGA | + | 7.05 | | HES2 | MA0616.2 | chr1:9170447-9170457 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr1:9170447-9170457 | GGCACGTGCC | - | 6.02 | | NKX2-3 | MA0672.1 | chr1:9170493-9170503 | ACCACTTGAA | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27376 | chr1:9170502-9171842 | Esophagus |
|
| | 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 |
| GH01I009110 | chr1 | 9170421 | 9176183 |
|
Enhancer Sequence | GCCTCTACTA AAAGAACAAA AATTAGCTGG GCGTGGCGGC ACGTGCCTAT AATCCCAGCT 60
ACTCGGGAGA CTGAGGTAGG AGAACCACTT GAACCTGGGA GGCAGAGGTT GCAGTGAGCC 120
GAGATTGTGC CACTGCACTC CAACCTGGGC GACAGAGCAA GACCCTGTCT CAAAAATAAA 180
TAAATAAATA AAACTAAAAT AACATACAGA ATGAGTGACC GAGTGGATCA AAGAATGGGT 240
TAATCTGTGG CCTTTTGCAG GCGTTTGCTT GTGGCCAGGA GGAAGCCCCT AGTTCCACAT 300
GTGCAGACTG GGAGGCAGGA ACAAGGAGGA ACTGGGCCAA GGTGTCAGAG GAAAGCCATT 360
CTTTCGTAGG CTCTCCAGCC AGCCCAGCCT ACTCATTTCT GAATTCTGGA AACCCCTGCC 420
ATTTAGGATA TAATAAATCA CTAGGAAAAG TTAGGTGAGT TATTTGCGTC ACTGATTGTG 480
AAATTCCACA GTCTTCCCTT CCCCTGGGGC AGCCCGGCCT TGGGTCTGTC CTCACCTTTT 540
AGCTAAATTC CTCAAGTTTA AGCAGCCACC ACAGGCCGTC CACCAGGGGG CAGGAGAGGG 600
CCATGACCAA GGACACAGCA GCCCTGTCTG CAGCAGCCCT GTGCCCCCAC AGGCCCTTAA 660
TCGGCTAAGC CTCGTTTCCT TATCTACAAA GGAGTAACAG GACCCGGCTC CTAACGGGGC 720
AGTGGGAACC AATGCACGAT CCGTGTAACA CAGCGTGTTG CATGGTGTCT GGTGCACAGT 780
AAGTGCCTGG TCCCCTCTGG CCCATCACTG GTTCTGTCCC CAGAGACGCA ACCTGTCCCC 840
TCGGGGGGCC AAACTCAATG CCAGGCCTTG CACCTGGGCA CAGCGGCCAT GCAGAGGGCC 900
CTGAGCTCTA AGGGCAGCGC 920
|
