| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04211 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:204314530-204315480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| E2F6 | MA0471.1 | chr1:204314650-204314661 | TCTTCCCGCCC | - | 6.14 | | NFE2L1 | MA0089.2 | chr1:204314932-204314947 | TCTGCTGAGTCACTT | - | 6.49 | | Nkx2-5(var.2) | MA0503.1 | chr1:204314791-204314802 | AGGCACTCAAG | + | 6.14 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_23313 | chr1:204314292-204315715 | Colon_Crypt_1 | | SE_24138 | chr1:204314390-204315044 | Colon_Crypt_2 | | SE_24138 | chr1:204315076-204315668 | Colon_Crypt_2 | | SE_28816 | chr1:204313934-204315755 | Fetal_Intestine_Large | | SE_33663 | chr1:204312332-204316029 | H2171 | | SE_50227 | chr1:204314309-204315837 | Sigmoid_Colon | | SE_65374 | chr1:204314364-204315978 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I204345 | chr1 | 204314729 | 204314928 | | GH01I204346 | chr1 | 204315077 | 204315668 |
|
Enhancer Sequence | AACCCAGGCT TCTTTGCTCA GCCCCCTGGC CCCACTCCCT TCGAGGTTTC TTTCCACTGA 60
GAACCCTCTC CACACTCCCC ATCTCTGCTG TGCCACTCTT CCAGAGGTCT CAGGTTCTCT 120
TCTTCCCGCC CCCCTCAGGT CTGGGTGCCA CCATGAGGCA GATGTCACAG GATCTCCCCG 180
TTACCCTCCC CCAGCGCCCA CGTGCACTGT GACCTGGGTT CAGCCTCACC CACAGCACAA 240
GTACTAGAGA GCTGGTGGAG GAGGCACTCA AGCATTTCCC TGAAAGAACA GCAGGGCCAA 300
CAATGACTCC TCCTGTCCCC TCTTCCCCCA CACTATGTTC TGCTCCCCCT GACCCCAGAG 360
CAGGTTCCCC CCAGCAAAGC CACTGGAGCA AACCCTCCTT TCTCTGCTGA GTCACTTGAC 420
CTTAATGGTA AGAGACCAGA AGCCCTGGAG AAAATCAGCT CACCCAACTT CCCAGTCGCT 480
CTCCACACTC ACATCTGAAC ACACACAAGA AAAGTGACCC CTGTTACAGG GATAGCAAGG 540
AAGAGCAGAA AGGTGTGGAG AGGAGTACAG AGAAAAGAAG AGAATGAGCG AAGCTCACCC 600
TGCTAGCCAC CACCAGATGG TTAAGCTGGC TTTAAGTGGG GACACTTGGT TTCTGGATTC 660
AGAGAAGGCC TGTTCTGCAA AGGGAAGCTA TGGCTCCTAG AGGAGCTGCT GCCCCATTGG 720
ATAGCCCCCT CCTCAATCAC AAGTGGGCAG CAGGGAGCAA GGAAGACTAC TGGCACTGGG 780
TGTGGTCTCT GATTCTCCCT CCACCCTAGC TCTGCCTCTA AGCCCTGCCT CAGCTGCTTT 840
GTGACTAGAT TTCTGCACTG TCTGACAGCC CCCTCGATTA TACCTAGAGC AGCTGACAGG 900
CCCTCTCTGT ATGCATGGGA ACATGAGAGC AGCAAACACT CTCACTCTCA 950
|
