| Tag | Content |
|---|
EnhancerAtlas ID | HS047-01067 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:40292280-40293170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr1:40292328-40292346 | GGAAAATGAAAGTCTGAC | + | 6.01 | | Mecom | MA0029.1 | chr1:40292994-40293008 | GTGATAAGATAAGA | + | 6.38 | | TFAP2C | MA0524.2 | chr1:40293019-40293031 | TGCCCCAAGGCA | + | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_23684 | chr1:40292306-40293327 | Colon_Crypt_1 | | SE_24232 | chr1:40292327-40293177 | Colon_Crypt_2 |
|
| | 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 |
| GH01I039825 | chr1 | 40290859 | 40293326 |
|
Enhancer Sequence | CCCAGAAAGC ACTTAAAATG TAAACAACAT GAATATAAAG TTATCTTAGG AAAATGAAAG 60
TCTGACCAGG AAATAAATGC AAAATCAGTT ACCTTTAAGA TAACCTCATA GGCCCATAAA 120
ACTAGAAAAA ACAAGGCAAC AAGGCCCCCA GCTGGTGAGG CTGTGGGGAA GCAAGGGCTC 180
CACCAGCCCC AGATGAGAAC AATGTGGCCG TCGAGGCCAG GAGCCCGGAA AGTGCACACC 240
CTGGAACAAG GAGCCTTGGG GGTAAACATA AATGAAATGC ACTTAGGCGA AAATGGAAAT 300
TTTTACAAGG AAATAGAGGT ATCTCAGGAA CCCAAGGAAG CACACTAGGC CTCAGGAGGG 360
TCGGGACCGA GGAACTGGGA AGTCAACAGG AATCTCTCTC TCCTTTCCTC ATCTGGGATT 420
CCCTCCTGCA TTGTCTGCTT TTCTCCTTCT CTGAAGATCA GCCTTCTCTG TTTTGTAGTG 480
CACCCATTCA TAACAACAAA TAGTTATTTC GTGTGTATGA CCAAACACAG TTCTTGTATT 540
TCTCTGTTCA AGTGTACCCA GCTAGGACTG AGCTGCAATT TGAAATTCCT GGGAGGAGTG 600
TGATTGGCCT GGCTGGCCCT CCGCTGGTCT AATAAGCTAG GAGGCAGGGT AGTCATTCCT 660
TTATGAAGTT ATGATCTCTG ATTCCTTTTT CCACAGGAAG ATAAATCAGT GAATGTGATA 720
AGATAAGATG GGGAGGGGAT GCCCCAAGGC AGAGAGACAG CTCAAAACTT CGAGCTCCAG 780
GCGCTGGTTC CAGCCAGAAC ATCCCGTTAA CCTTTTTCCT GCTTCCACAG TCCACATCCT 840
TGTTATGCCT TTACAGTCTA TTTTCACAGA GCAGCCAGAC TTATCTTTTA 890
|
