| Tag | Content |
|---|
EnhancerAtlas ID | HS182-13467 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:242100820-242102180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr2:242102044-242102059 | AGGTCAGAGTGCCCC | + | 6.65 | | ESRRB | MA0141.3 | chr2:242101015-242101026 | TTTGACCTTGA | - | 6.14 | | Esrra | MA0592.2 | chr2:242101016-242101027 | TTGACCTTGAA | - | 6.14 | | KLF4 | MA0039.3 | chr2:242101950-242101961 | GGAGGGTGTGG | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 242100975 | 242101658 | | chr2 | 242101722 | 242102041 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I241161 | chr2 | 242100769 | 242102279 |
|
Enhancer Sequence | TCTTCGAGAT GAAAGTTTCC CAAGCCCAGC AAAGTGGTCA CTTGGAGTGA ACTGATGTAC 60
ATACCGGGGG CTTTAGAAAA CCTCTTGATG CTGACACACT CCCAAAGGCA GTGCTGAGTT 120
GGGCCTTCCT CCCTGGACAG CTTTATACTC CTGGACACCG TCCCCAGCAG GATTAGATCT 180
GTTCTCCAGG ATCCATTTGA CCTTGAAAAC GTGGGACAGA ATGGAAATAA AAGAATTTTG 240
AAAAGTGATC TGGTGTTCCA CAGAAGCAGG ATCAAGTCTT CACCAGCTGA CTCATAACCA 300
CCGTCATGTG CTGGAGGGGA ACTTGGGAGG GCGTCCCAGG AGGACTGACA TTGGAGGTGG 360
ATCTGCCAGG CAGGGAGGAG GGAGGGTTCC CGTGGGCAGG AAGGAGGACT TCTCTCAGCC 420
AGAAGAACAC TTGAGCCCCG TGCCTGGCTC CTAATCAGGG TCATGGCACG GAGCCTTTGC 480
TCCCCCGGCC TGGCTTAGTG GCTTTGGCAG CTGTGTCTAA GCACATCCGC CCCTGCCCAT 540
GTTCAGAATG CCCCTCTACT TGGCTTCTGG AAGTATTACA GCATTCTCTG TCTGTCCTGG 600
GCCCTTGAGA GCTTGGACAG GATACAAACC AAGGGAGGGT GGTTTTGGCA ACAGTCTCTT 660
GACAGTTATT GTTAGAGATG TCATGGCCAC AAATAGCAAA GCAGCACATT TAAAACTAGA 720
GAGCAGCCCA GATGTCCGCA TTTTACCAAG TGTCTCACTA TGGAACTTTC TAGGGCAACA 780
GTGGCTCATC ACAAATTAAT GCAGGCTACA GCATGTGAGG ATGCCCCTGC CCCCGCCAAG 840
TCCTGCAGTG GTGTGTGGAT TAGCACACCA TCTCCCCTCC TAGAGTCCCC ACCTGGTTAG 900
CATGCACCTT ATCTGGTTAT TTTGTGTCTG CTGAAATATT TAAAGAATGA CTTGTTCTGA 960
GAGAGAGTGA ACTGACAGAG GAGGGAAACT GAAGTCAAAT CAATAAACAG TCATTAAACA 1020
TCCTGCTGTA GGCAAGTCAC CATGGGGAGA CCAGACAGGG CAGCGTGGTC ACTGCCTCTG 1080
GAGGTTTATG GTTGAATAGA GGAGCACACG ATCACAGCAA GAGTGATGTA GGAGGGTGTG 1140
GAAACTGGGC AAGAGGGGCA GAGTGCTGTG GTGTGAGGGC CCCCCAGGAA TCCTAAGTGA 1200
GGGTCCCAGG ATTTCAAAGA CTTGAGGTCA GAGTGCCCCG TACCTCTCTT CTGTAGAGAC 1260
TGAGGCTCTT GGGAGGACTT TTTTTTTTTT TTTTTGAGAC GGAGTCTCGT GCTGTTGCCC 1320
AGGCTAGAGT GCAGTGGCAC AATCTCGGCT CACTGCAAGC 1360
|
