| Tag | Content |
|---|
EnhancerAtlas ID | HS047-04438 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr10:81117680-81119000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr10:81118496-81118506 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr10:81118496-81118506 | GGCACGTGCC | - | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_24675 | chr10:81117939-81118347 | Colon_Crypt_2 | | SE_24675 | chr10:81118425-81119200 | Colon_Crypt_2 | | SE_25306 | chr10:81118435-81119205 | Colon_Crypt_3 |
|
| | 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 |
| GH10I079358 | chr10 | 81117879 | 81119431 |
|
Enhancer Sequence | GGGAGCTCCT CGATAGCGCT GGTCAAAGTG GCCAGCCAGG CATGGTGGCT CATGCCTGTA 60
ATCCCAGCAC TTTGGGAAGC AGAGGTGAAC GGATTGCTTG AGCCCAGGGG TTTCAGACCA 120
GCCTGGTCAA CATAGTGAGA TCGCATCTCT ACAAAAAAAA AAAAAAAAAA AAAAAAAAAA 180
AAAAAAATTA AAACTTAGCT GGGCTTGGTG ACATGTGCCT GTGGTCCCAG CTACTCGGGA 240
GGCTGAGGTA AGAGGATCAC TTGAGCCCAG GAGCCGGAGG CTGCAGTGAG CCATGATCAT 300
GCCACGGGAC TGCAGTCTGG GTGACAGAGC AACACGCTGT CTCAAAAAGA GAAAAGAAAA 360
AGTGGCTCCC CCTGTCTTTG CCTATGCAGG AGCCTGTGAA GGAAGAAGCT CCTAGAGGGG 420
TGGAGGCCCC AGCTCTTGTT TTGTCATCTA GGAGGAGGGG CTGCCTTGGG TGGGTCTTGG 480
ATGGAGTGCA TTTCTCAGTG AGTGGATTGC GGAGGCCAGA AGTCAGCTCT ATGTCCAAGA 540
TTCTTCAGAA TATGGCAGGT AGAGAAAGTC TTGGGTCCAT TCTGCCTCCC AGATCACCCA 600
GCCTGTAGAG GCTGTCCAGA ATTATGCTGA TAACATTATT GCTATTCTAT CATATTGTGA 660
TCGTTAATTT TATGGGTCAA TTTTTTTTTT TTGAGATGGG GTCTCACTCT GTCACCCATG 720
CCGGAGTGCA GTGGCACAAT CATAGCTTGC TGTAACCTCA AACTCCTAGG CTCAAGCAAT 780
CCTTCCACCT CAGCACCCTG AGTAGCTGGG ACTACAGGCA CGTGCCACCA TGCTTGGCTA 840
TTTATTTTTT ATTTTTTTAA AAGATGCGGG TCTTGCTGTA TTTCCCAGGC CAGTCTCTCC 900
TGGCCCCAAG TGGTCCTCCC ACTTCAAATT CCTAAAATGT TGAGATTATA GGTGTCAGGC 960
ACCACACCCA GCCTTATGTG TCAACCTAAC TGGGTCACAG AGTGCTTACA CATTGGGTCA 1020
GACACTATTC TGGGTGTGTC TGTGAGGGTG TTTCTGTCTA AGATTAATAT TTGCATAGCT 1080
AGACCGAGTA AAGCAGGTGG TTCTCCCTCG TGTGGGTGGA CTTCGTCCAG TCAACTGAAG 1140
ACCTGAATAG AACAAAAGGC TAAGAGGGAA CGCCTCCTGC CTGACGGTCC TCAGCTGGAA 1200
CATTGGTATT TTCTGCCTTT GGACTCAAAC TGAAATGTTG GCTGTCTCAG GGTCTTGAGC 1260
CTGCCAGCCT TCAGACTGGA ACCTACATTG GCTCTTCTGG TTCTCAGGCC TTCAGACTCG 1320
|
