| Tag | Content |
|---|
EnhancerAtlas ID | HS182-01742 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:203575990-203577100 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr1:203576594-203576605 | GATGAGTCACC | - | 6.32 | | Foxd3 | MA0041.1 | chr1:203576399-203576411 | AAACAAACAAAC | - | 6.32 | | JUND | MA0491.1 | chr1:203576594-203576605 | GATGAGTCACC | - | 6.62 | | NFIC | MA0161.2 | chr1:203576579-203576590 | TCTGCCAAGAA | - | 6.02 | | RREB1 | MA0073.1 | chr1:203576623-203576643 | GGGCTGGGGTGGGTTGGGGT | - | 6.03 | | RREB1 | MA0073.1 | chr1:203576622-203576642 | GGGGCTGGGGTGGGTTGGGG | - | 7.16 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25758 | chr1:203575191-203577246 | DND41 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr1 | 203576120 | 203576183 | | chr1 | 203576282 | 203576863 | | chr1 | 203576404 | 203576703 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I203606 | chr1 | 203575245 | 203577382 |
|
Enhancer Sequence | TGTGCCTATA ATCCCAGCTA CTCGGGAGGC TGAGGCAGGA GAATCGCTTG AACCAGGGAG 60
TCGGAGGTTG CAGTGAGCCG AGATCGCGCC ACTGCACTCC AGCCTGGTGA CAGAGTGAAA 120
CTCCATCTCA AAAAAAAGAA AGACCTTGTT AGATAACTTA GCTAGGCATG GTGCCAGGCA 180
CCTGTAATCC CAGCTACTCG GGAGGCTGAG GCAGGAGAAT CATTTGAACC TGGGAGGTGA 240
AGGTTGCAGT GAGCTGAGAT CGCACCATTG CACTCCAGCC TGGGCAACAA GAGTGAAACT 300
CCATCTCAAA AAAAAAACAA GAAAGACATT GTTAGATAGC ATTGAGCATA TCACTTAAAT 360
GGCCTTGGCT CACCCCCTGG GGAAATCATG TTCTTTCAAA GACACTATAA AACAAACAAA 420
CAAAAAAAGC AACAGTAGCT ACAGAGTTCC TGCTCCAGCA ACCAGGAGCC TTGAGGCAGC 480
ACAAGGACAC CGGGGCGGGA GCGTGGCCCA AGAAGCAGAG ACAGCAACAA CAACAGGATG 540
ACTTCATTTA CTGAGTTATC AAAAACCACA ATGTCTGAAA ACCACAATGT CTGCCAAGAA 600
AGAGGATGAG TCACCAAGAC CCACAGGAAA GAGGGGCTGG GGTGGGTTGG GGTGGGCAGC 660
ATGGCATGAT GAGAAAAGCA AGTATTTTGA CAGCACACAG ATTCAAATCC TGACACATCT 720
CTGAGGCCTT CAGCTCTCTG GGTCTCAGCT TCCTTTATCT TTAGTTTTTA TTTATTTTTA 780
TTTCAAAAGA AATGAGATGG AGTCTTCTCT GTTGCCCAGG CGGGAGAGCA ATGGTGCAAT 840
CTTGGCTCAC TGCAACCTCT ATCTCCTGGG TTCAATTGAT TCTCCTGCCT CAGCCTCCCG 900
ATTAGCTGAG ATTACAGGTG CATGCCAGCA CACCGGCTAA TTTTTGTATT TTCAGTAGAG 960
ATGGATTTTA CCATTTCGGC CAGGCTAGTC TCGAACTCCT GACCTCAAGT GATCCACCCA 1020
TCTGGGTCTC CCAAAGTGCT GAGATTACAG GTGTGAGACA CCATGCCCAG CCCTCAGCTA 1080
CCTTATCTTT AAAAATGGGA AAGAGCCAGG 1110
|
