| Tag | Content |
|---|
EnhancerAtlas ID | HS044-07883 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:238357500-238358790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr2:238358053-238358064 | AAAGATAAGAA | - | 6.62 | | HSF1 | MA0486.2 | chr2:238358726-238358739 | GAAAGTTCTAGAA | - | 7.04 | | NEUROG2 | MA0669.1 | chr2:238357710-238357720 | AACATATGTC | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_54889 | chr2:238357431-238358559 | Stomach_Smooth_Muscle | | SE_55655 | chr2:238357726-238358749 | u87 | | SE_67451 | chr2:238357726-238358749 | u87 |
|
| | 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 |
| GH02I237449 | chr2 | 238357760 | 238362106 |
|
Enhancer Sequence | CTCTACAAAG GCCCAGGCCC AGGCAGCCCC TCCCTCACAT CTGGAAGGTT CTGAGCACAA 60
GCAAACCCAC GGTCCTTAAT ATTTCCTGAT CTGAGCAGGT TTTTAACCAA GCTGGAAGAG 120
ACCACTTAGA AAAGAAGGAA AATAAAATTC CCCTTCAGAA TGCCAAGATG GAGAGATTTA 180
TCTTCATTCT AAAAAAAAAA AAAGTGGAAA AACATATGTC TGTGGCCCAT TTTGAGTGGA 240
AAGTTTTATT TATTCAACTG TTTATTGTTA TTTCTCTGCC CACCACAGCA GGGTGAGGGC 300
AAGTCTGATC TGCGGCCTCA CCCTCTCCAA GTGCCTCCCC CAACCGCGCT CCCTTCCCCT 360
CCCCACTCCC GGGAGGACCG AGTTGGTTCC ATCCTCCCTC AGACCCAGCC AGGAAGCATG 420
CTGTGCCCTC TCCTTTCTCC AGCACCTGAG CCTGGAGAGA GGCCCTGTGT GCCAGGGGCC 480
TCCGTGGAAT CCTTGACAGC TCCCCCAACT GCCCAATGCC CACATCAACC TCCTCTAAGT 540
TAGCACTTTT GTCAAAGATA AGAAAAGTAT TTTCAGGAAG CCCAAGTGTT TCCTGTTTGG 600
CAGAAGCCAG GCTGAAACGC CCCAACTGGG AGCAGGGAAT CGGGCTTGAC CTGCATGTGT 660
TTACAGAAGT CAGCTCAGAA GGAAGTGCGG TCCAAGGGTC TTCTTGTTCG TTTATTGAAA 720
AGGCCATTAA CGGTTTTTGT CCATCTCTGC TGCTGCTGTT GATGCTGTTT GCATAAATGA 780
CACCAGATCC TGCAAACCCT GCCAGTCTGG TGTGTCACTC ACTAGAGCAC TGGCTGCTCT 840
GTAGCTTTCC AGCCAAGGGA ACACATCGTC CTGCCTGCTT TCTGCTATGG ATCCAACTGG 900
TTCTTCTTGT GCCAAAAATG ACTGCATGGT GTCATATGCA CGGCACTCCA TTTGATCGTT 960
TATTCACCAA GCCTGTGTTG AGAAGCTTCC CTGTGTTGGA TGCTGCTCTC TGATGCCCTG 1020
GGAGACAGGA GACAGGCTAA GGCTCCTGCC CTCAGGGAGG TTCCACTCTA GAGAGGGATC 1080
CAGATACATA AGGGAGACCC TGTTGTGTTA AAGTGAGAAG AGCTAGGACA AAATCAAGTA 1140
GGAGGGGCAG AGGAAGTGTG AGGGGAGGGC TGGCATTTTA GAGGGAGAGG CTGAGGCCAG 1200
GGAGGGCTGA CTAGAGAAAT GACACAGAAA GTTCTAGAAG GTGAGGTGGG AAAGTGGAAC 1260
CAGCTTGCAG CCATCACTCT GAGTGTGAGA 1290
|
