| Tag | Content |
|---|
EnhancerAtlas ID | HS105-00234 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr1:6329650-6331040 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr1:6330360-6330380 | GGGTTGGGGGTGGGTGGAGG | - | 7.13 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_24674 | chr1:6328963-6332343 | Colon_Crypt_2 | | SE_37032 | chr1:6329131-6331255 | HSMMtube | | SE_67116 | chr1:6327167-6334026 | H2171 |
|
| | 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 |
| GH01I006268 | chr1 | 6328561 | 6334156 |
|
Enhancer Sequence | CCAGGCTGAG GGAGAATCTG GTGCCCAGCA ACGGGCCCCA AGGCGGCTCT GATGTGGCCC 60
TGCTCTTTAA TATTTGCAGC AAACTCATCA GCCAGGCTCT GCCCTCAGAC AAAGCAAATG 120
CTGTCTGATG ATGGATGGAT GTGTGGGAGC CTGAGAGCCT GTGAGGGCCC CACTGCTCTT 180
CCCGTCTCCC GGGATGGTAG TATCTGCTGG ATGTTCCAGG CTCTGAGACA GAGTCCAGAC 240
CAGCCCAGGA GCCTCAACGT CACTGCGTGG AGTGCCCGCC CATAAGCGCT GCCCTCCCAA 300
GGTGCGGGCG GCCTTCCTCC CTGAGTGCCC AGGGGCGCCC TTCCAGGGTG AAGGTTTATG 360
AAGATGGCAG TCAAGGGCAG GGATGTCCCA GGTGCCTGAG GACCCAGGCT CACCACCCAG 420
GGGGAGGTGG AACAAAGGGC CGCGGGGCGG TGTCTGTCCC ATGGTAGGTT ACGGGCTCAC 480
TGCTGGTGGG CAGCCAGCCT CCCCAGGTCA TGGCTTTGCT AAATAGTTCT CCTACCCAAG 540
TGACAAAGGG GCCACCCTGT CCCGCTGGGT GAGAAGCTGA CAGAGCAAGA CAGATGTCTC 600
CAGCACAAGG CCCCACCCAC GGCCCGGCTG CTGCCTCCTC GCAGCCATCT CCCTCCACCC 660
AGCAAAGTAA ATAAATGCAT ACGCTGTTGG CTGTTGCTGT TTTTAATGGA GGGTTGGGGG 720
TGGGTGGAGG ACGAAAGAAC GCTCTGCGGG AAGACAGATG TCTCTCTCAA GTCCCCGAGG 780
CTGCTGGTGG GGGAAGGACT GGAGCCTCTG GGGCACTGGC CAGTGGTGCC AGCTGCCGGG 840
CACCCACCTG TGGCCTCAGG CAGGCTCCTC CGAGCCTCTG GGGCTCCCCA AGAATATGCC 900
AGAGAGAAAG GATGAGGTGG CAAAGGGCAG CTCAGGGCAC ATGACCCCCA TGTATCCCGG 960
GCACCTGCCT GATGGAAGGG ATGGGGCAGC ATGGCCAGGA GCAGGACTCT GAGTCCCACG 1020
GGCCCAGCTG TGTGGCCCAG GGCCAGGTTT GTTCACCTGG AAACAGGAAC TCAACAAAGT 1080
GACATGGCAA AGTGCTTCCT ATGGTGCCGG TGCACGTGAG CTCCTACGTG TGTGTGCACA 1140
TGTGTCTGCG GTCCCTGGTG CATGTGTGTG TGTCTGTGTG GTGGTCCTGC TGTCCTCAGA 1200
AATACCTGAG GCCAAGTGCA GCCTGGGAAC TGCTCCAAGG ACTGTCCTGC TGGTGTGTGG 1260
CTGCCCCAAA GGAGGGCCAG ATGGCCCGGG GTCACCTTAA CGCAGCGGGC CCTTTAGGAT 1320
GTCACACCCA CACATGGGGA CGCAGGGGTG GGGAGGGTCC CAAGGTAGCA GGTTGACAGT 1380
ACGCTCCCTC 1390
|
