| Tag | Content |
|---|
EnhancerAtlas ID | HS048-02006 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:110074630-110075730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:110075083-110075102 | CACTGCCCCCTTGTGGTTG | - | 6.88 | | HNF4G | MA0484.1 | chr1:110074957-110074972 | AAAGGTCAGAGTCCA | + | 6.07 | | Hnf4a | MA0114.3 | chr1:110074958-110074974 | AAGGTCAGAGTCCACA | + | 6.12 | | Nkx2-5(var.2) | MA0503.1 | chr1:110074637-110074648 | AGCCACTCAAG | + | 6.62 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_08699 | chr1:110071934-110076498 | Brain_Inferior_Temporal_Lobe | | SE_30139 | chr1:110070015-110076037 | Fetal_Muscle |
|
| | 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 |
| GH01I109527 | chr1 | 110070488 | 110076210 |
|
Enhancer Sequence | AGAGAGAAGC CACTCAAGGA CAGCAGCTGC TGACTCAGAC GCTCAAATTC TCGGGCGGAA 60
AAGGACCTTA GAGAATGCCT AAAATCGTGG CCCAATCCCT CATTGGAAGC TGGGGCTCCG 120
AAAAGCCGGG GCTCCGAAAA GCTGGGAGAG CAGCCCAAAG CGTACTGCCC ACTAAATGTG 180
GATGCACGCT GGACCGCCGG TTCAGGCCTC CTTCTGGGAC ACCAGTCGGC CCATCTCTTC 240
CTCATAAGCT CTTAGGAGTA GGAGGGATTT TATTTAACGA GCCAGGGCCC TCTCGCCTGG 300
TCCTCCCAGC CGACTGTGAT GGTGTAAAAA GGTCAGAGTC CACAGGACCA CCATAGGACC 360
ACGGTCTCCA GGAGGGAGAA GGCAGGTGGC GGTTGGGCGG GGAGAAGCCT GTCACCGGGG 420
ACTGCAGTCA ACTCTTTGCA GCTCTGTGGC CAACACTGCC CCCTTGTGGT TGCTGGCTGT 480
CAAGGCAGTC TGGGGGCCGG AAATGGAGAG GCTTGGGTCC TCTTTCCCAC CCAGGACCTC 540
ACCCTCTAGG AACCCCTGCC TCGTGCGATG CTGATTTACA TCCTCCAGGG ATACCCCTCC 600
AGGGGAGGCC ATCCAGGAGA CTGAGCTTCC ACTTGCCATT CTGCAGTAGG GTCCCCAGGC 660
ATGTGGGTGA GGGCTGACCA CCTCCCGGGC GCCCAGAAAC CCCAGGGGCC ACTCACAAGC 720
TATCTCTGGA TCCCCAAGGA GTCCCCCAGA GTTCTAGGTC TGGAAGTCTG TCCCTCCCTT 780
CAACCAATGG GCATAAGAGT CGGGGGGTGC TATTTTTAGG TGGGGCAGGA ACGCAGGGAG 840
AGGACTTTGG AGGGAAGGAG ATGTCTGGGA AAGAGGTCAC AGGACCAGTA TCATTGTGCT 900
CAGTGGTGTC CAGCCTGGAC AGGGAAGAGT CAGGTTCCCT TGGGCTCAGC AGGGGTTGGC 960
TTGGCTGAGG ATGAGATGGT TAGGGGCGAC TGACCCAGAG ACATAGAGCA GGGGTGCCCC 1020
CCAGAGTCAG ACACCAGGCA CTGCTGGGAG TGCTCTGTGG AGCTCTCAGT TGGGAAACCC 1080
AGCCCAGTTC TTTTTGTTTT 1100
|
