| Tag | Content |
|---|
EnhancerAtlas ID | HS047-00912 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:33177520-33178670 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:33177929-33177948 | CTGCCTCCAGGGGGCGCCG | + | 7.13 | | EGR4 | MA0733.1 | chr1:33177702-33177718 | GATTGGGTGGGCGTTA | - | 6.5 | | SOX10 | MA0442.2 | chr1:33178618-33178629 | TCCTTTGTTTT | - | 6.32 | | Sox3 | MA0514.1 | chr1:33178619-33178629 | CCTTTGTTTT | + | 6.02 | | Stat4 | MA0518.1 | chr1:33177688-33177702 | CTTCTAGGAAATGA | + | 6.69 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_00938 | chr1:33178029-33178382 | Adrenal_Gland | | SE_23116 | chr1:33178028-33178421 | Colon_Crypt_1 | | SE_65538 | chr1:33177560-33178568 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 33177600 | 33178437 | | chr1 | 33177693 | 33178298 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I032711 | chr1 | 33177402 | 33178550 |
|
Enhancer Sequence | GCACTTGCCA CCACGCCAGG CTAATTTTTG TATTTTTAGT AGAGACGGAG TTCCACTATG 60
TTGGCCGGGC TAGTCTCAAA CTCCTGACCT CAGGTGATCC ACCCGCCTCG GCCTTCCAAA 120
GTGCTGGGAT TACAGGCGTG AGCCGCCGCG CCTGGCCCCC TGATTCTGCT TCTAGGAAAT 180
GAGATTGGGT GGGCGTTAAA TGAGAAAATG TGCAGGAAAT GCCCAGCCTT TTGCCCAGTA 240
TACAAGAGAC ACTTGATAAG TGTTCTTCTC TTTATTTCCT TCTTTCTCCC TGCCCTCTGG 300
GACCGCTGTC TGGGAGCCAT TGGGGCCTAC CCGGTGCTGA CCACCAGCCA CCGCTTCAGA 360
GGAAGCTGCG TTCAGGGTCG TTCCTCCCCA GGTCGGGCAA TGCCGAGCAC TGCCTCCAGG 420
GGGCGCCGCC ACGCCGACCC CGCGCCCCGG GGGTTGTCTT TTCCGCCGCA GCCGCGCGGG 480
GCCGCCCGGG CCCTGAGTTT TCAGGACCGA TGGCGCGCCG ACAGTGGGGA GGTCGGCGTC 540
CCAGCTGAAT CAAGGACGTC CTTTAGCACC GCAGTGATAA TGAACACACA ACAATAATAG 600
CCGCAGATCC ACCCATAGCG AGCTGCTGGA GTTTAAAGGG CGCATGCGCT TGCTGGGAGG 660
CTGTGGGACT CAGGGAAGGT GCCAGGCCTT AGACTCTGAG CTGGGTTCGA ATCCAGAGCA 720
GAGCAGTCTC TCACGTTTCC CCGCTCTGTA CCCTTAGGCT TCTCTGAGCT TCTGCTTCCT 780
TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT TGAGACGACG GAGTCTGGCT GTGTCGCCCA 840
GGCTGGAGTG CAGTGGCGCG ATCTCCGGTC ACTGCAAGTT CCGCCTTCCA GGTTCACGCC 900
ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG GGACTACAGG CGCCCGCCAC CACGCCTGGC 960
TAATTTTTTT ATATGTTTTT AGTAGAGACG GGGTTTCACT GTGTTAGCCA GGATGGTCTC 1020
GATCTCCCGA TCTTGTGATC CACCGGCCTC GGCCGCCCAA AGTGCTGGGA TTACAGGCGT 1080
GAGCCACTGC GCCCAGCCTC CTTTGTTTTC AAATGGGAAA TGTATTATAG TTCTTGAGAG 1140
GAATAAATGA 1150
|
