| Tag | Content |
|---|
EnhancerAtlas ID | HS051-03294 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr10:70984190-70985570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Atoh1 | MA0461.2 | chr10:70984730-70984740 | AACATATGTT | + | 6.02 | | Atoh1 | MA0461.2 | chr10:70984730-70984740 | AACATATGTT | - | 6.02 | | Zfx | MA0146.2 | chr10:70984282-70984296 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27984 | chr10:70979065-70991295 | Fetal_Intestine | | SE_28850 | chr10:70979061-70987098 | Fetal_Intestine_Large | | SE_53047 | chr10:70984148-70986283 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CACCACGCCT GGCTAATTTT TGTATTTTTA GTAGAGACAT GGTTTCACCA GCTTGGCCAG 60
GCTGGTCTCG AACTCTGACC TCAGGTGATC CACCCGCCTC GGCCTCCCAA AGTGCTGGGA 120
TTACAGGCGT GAGCCACTGC GCCCGGCCTT GGTAGAGATT TATGGTTCTC CATAGTCAGG 180
ATTATTTCCT GAGAATAGGT TCTGGAAATG AAAGCCCTGG GTCAAAGAGC GGAATTTTTT 240
ATGACTCTCA TTCCTAATGT GAGACCTTTG GACTAGACGA GCTCTAAGGC CCCTCCAGCT 300
CCCACCTTCT GCAATTCAGT CTTGAGTCTT GAATGTTGGA TTTGCTCTTT CTAAGTGAAA 360
CGGGCTGCTG GTTGGCTTTC TTGCTTAGAC GATATCTCCC ATGATGGTTT GTGTGTCTCT 420
CCAAAAGTGG GCTTGGTTTT CTGCAGCACC AGTACTCTCC CTTAGTGCCT GGGACGTGTG 480
TCCCTGGTTA CACATACCCC ACATGACTTG TTTGGATTGA AAATAGGTGC TTTTTGTCCC 540
AACATATGTT TCACTTTTCC CTTCTAACAA CTGTTCCTGG TGCTGTGGCA GATACAGAAG 600
ATCAAAAGGA AACTGTTGCT GAGTTGACAT TCTTTCTGTC ATAACCTCAA CTTATTGAAA 660
GAGCAGCAGC AAACCAAGTG CTCAATGACC CCATTAAACC CCAGTCGCAA ATGACCCCAA 720
CTGGGTCTCA AAAAACAGGA CTTACATGGC AGGGATAACA TTGTGTGGAT GCCTGGAGTT 780
TTTTATACTC TCAGGCTAAG CAAAAATGAT CAGTAGGTTC AGGGGCACTG TCTGAGAGCC 840
CTTTGGGTAG GAAAGAATCA AGTTTGGTTC CCACATACAG CATCCCACCC TTCCCCAACC 900
CCAATTACTT GGGTCACGTC CTTTGCATCC AGTTTTCTCG GCTTGTGTGT GGCTGTGCCA 960
ACCAATTAGT CATAAACAGC CTTGGGGGAA CAGGAAGCCC TTAATGAAGC CTGACCTGGT 1020
TCCATCCTGT TTCTCAAATA TGCTGAAAGC TCAATTGTCC TTTTTTGCTA ATGGCTGTCT 1080
GATGATTTTC TGGTCTTTCT CTGGCCCCCG AGTCCCCGGA GCCATGGTAC CATTTCAGTG 1140
TCTTGGGTCT GTTCGTTGTC ACGAGACTGA GCTGGGTCCT GGCCTCTGAG GCCTGGCTGA 1200
TGACCGGGCC CCTGTCCTAG CGCGAAGGTA ATGTGAGCCC TGTGCATTTG GTATAATTTG 1260
TCTGTCGGGC TTATGCATCC CCGACAGAGC TGTGAGCCAA AGCCAGGCCA TGGGGGTGAG 1320
TGATCTAGAG CCTATGTTAC AGTCCCACGT AGCCACAGCT CTGCAGCCCT CTCACCTCAC 1380
|
