| Tag | Content |
|---|
EnhancerAtlas ID | HS138-30162 |
Organism | Homo sapiens |
Tissue/cell | MSC_BM |
Coordinate | chr4:79542850-79544160 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:79543507-79543525 | GTAAGCAAGGCAGGAAGC | + | 6.14 | | ZNF263 | MA0528.1 | chr4:79543365-79543386 | GGAGCAATAAGAAGAGGAGGA | + | 6.17 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28231 | chr4:79542397-79553389 | Fetal_Intestine | | SE_28631 | chr4:79542204-79553895 | Fetal_Intestine_Large |
|
| | 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 |
| GH04I078621 | chr4 | 79542568 | 79553114 |
|
Enhancer Sequence | ATCTATGCTG CCCCTGAGAC CCCCAGGAAG TCTGAGCCCC AGCTGCCCGC AGTGACAACT 60
GACTCACAAC ACACCCTGTA CCGGCTTTCT TTCTTTTTCT GTCTCACTTC TGCACTCACT 120
TCCCAGTGCT TCCTGGGATC CCTGGATCCT TTTCTCAGCA TCTGTTTCTG GAGGGACACA 180
TCCCAAAATA GGAAGGACTA TTTTCAGTAG TCACTATAAA GTAGGAGGTG TAACTGTGTG 240
TAACTTTGTG GGGTTACAGG GTGGAGGAGT TGAGAGAAGA AAACGGAGGC TTTTAGGGTA 300
GAAATCCTCT AGAACAGTGA TTCTCTGTGT TGGCGTGCTA GGGAGTCACC AAGTGTTTTG 360
GAAGTGAAAT GGAGAGGTAG GAGGAGCACT GGGGTGGCTC AAGTTAGATG GCTCTGGGAA 420
GGAAATGAGC CACAGCTTCA AAGTTCCACC TCTTTCTTCA AAGCACAGTT ACCTGGAAAC 480
ACAAACGAAA ACGAATGAGA GGAAGATGAA GAATAGGAGC AATAAGAAGA GGAGGAGGAA 540
ATCCCATCTA ATTTTATCTA CCACATTGCC ACCTTATTAC TACTTTACAT TTATTTCCAT 600
GGGTTCTTTG GAAGTGAAGT CCAGAATTTA GGGGCACACA GGGAGTCTAT GATTCTAGTA 660
AGCAAGGCAG GAAGCAGTGA AGGCAAATAG AATTAGTGAA TGAAATGGGA TAGATCATGT 720
GACGCAGGAG AGGTTCCAGG GAAGCTAGAG ATGGGCTTCC TGGGTGGGGT GAAGGAGATG 780
ACAGGCTGTG GCTGCAAATG GGATAATAGA TCTCAGAAAC AGAGATTACC CTGAGTGTTA 840
ACGACACTGA CTAAGGCAGG TCAAAGGTGG AGGTCTTCAA CCCAGGAAAT ACCTCTGGGG 900
TAAAGGAATC TAAAAGGTTA ATGTGGATTC CAGAGTCAAT ATAGATTATG GCAAAGGGCA 960
GGGCAGAGGA GCAGGACTGA GTCCGCTGCT GAAGTAAGCT TGGGAAGTGA GGATGGAATC 1020
TGGTGAGTCA CAGCATTGAG AACTGCACAG TCTTCAACTG GGCAGAGGGT GAGAGTGGGT 1080
GAGGGTAGTT CAAGGGTGAG AAAGCACACT GGAGGGAGGA AAGAGCTGGC CGCTCCACCT 1140
CACCCGCTGA CTTGAGCAGA GAAGATAAGG CTATCATGCT GAAAACAGTT GGGAGAACAG 1200
TGATTTCACA GGAGAGCATC TTTCAGGCCA GACGGCAGAA GAAAGAGGAT CCATGTGAAT 1260
GGGGACTGTG ATGGTTAATT TTCTGTGTCA AATTGGCTAG ACCACAGTAT 1310
|
