| Tag | Content |
|---|
EnhancerAtlas ID | HS116-20421 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:242100770-242102200 |
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 | ACCGGGGCTT TAGAAAGCCT CTTGATCATG GTCATCTTCT CTGGCATGCT TCTTCGAGAT 60
GAAAGTTTCC CAAGCCCAGC AAAGTGGTCA CTTGGAGTGA ACTGATGTAC ATACCGGGGG 120
CTTTAGAAAA CCTCTTGATG CTGACACACT CCCAAAGGCA GTGCTGAGTT GGGCCTTCCT 180
CCCTGGACAG CTTTATACTC CTGGACACCG TCCCCAGCAG GATTAGATCT GTTCTCCAGG 240
ATCCATTTGA CCTTGAAAAC GTGGGACAGA ATGGAAATAA AAGAATTTTG AAAAGTGATC 300
TGGTGTTCCA CAGAAGCAGG ATCAAGTCTT CACCAGCTGA CTCATAACCA CCGTCATGTG 360
CTGGAGGGGA ACTTGGGAGG GCGTCCCAGG AGGACTGACA TTGGAGGTGG ATCTGCCAGG 420
CAGGGAGGAG GGAGGGTTCC CGTGGGCAGG AAGGAGGACT TCTCTCAGCC AGAAGAACAC 480
TTGAGCCCCG TGCCTGGCTC CTAATCAGGG TCATGGCACG GAGCCTTTGC TCCCCCGGCC 540
TGGCTTAGTG GCTTTGGCAG CTGTGTCTAA GCACATCCGC CCCTGCCCAT GTTCAGAATG 600
CCCCTCTACT TGGCTTCTGG AAGTATTACA GCATTCTCTG TCTGTCCTGG GCCCTTGAGA 660
GCTTGGACAG GATACAAACC AAGGGAGGGT GGTTTTGGCA ACAGTCTCTT GACAGTTATT 720
GTTAGAGATG TCATGGCCAC AAATAGCAAA GCAGCACATT TAAAACTAGA GAGCAGCCCA 780
GATGTCCGCA TTTTACCAAG TGTCTCACTA TGGAACTTTC TAGGGCAACA GTGGCTCATC 840
ACAAATTAAT GCAGGCTACA GCATGTGAGG ATGCCCCTGC CCCCGCCAAG TCCTGCAGTG 900
GTGTGTGGAT TAGCACACCA TCTCCCCTCC TAGAGTCCCC ACCTGGTTAG CATGCACCTT 960
ATCTGGTTAT TTTGTGTCTG CTGAAATATT TAAAGAATGA CTTGTTCTGA GAGAGAGTGA 1020
ACTGACAGAG GAGGGAAACT GAAGTCAAAT CAATAAACAG TCATTAAACA TCCTGCTGTA 1080
GGCAAGTCAC CATGGGGAGA CCAGACAGGG CAGCGTGGTC ACTGCCTCTG GAGGTTTATG 1140
GTTGAATAGA GGAGCACACG ATCACAGCAA GAGTGATGTA GGAGGGTGTG GAAACTGGGC 1200
AAGAGGGGCA GAGTGCTGTG GTGTGAGGGC CCCCCAGGAA TCCTAAGTGA GGGTCCCAGG 1260
ATTTCAAAGA CTTGAGGTCA GAGTGCCCCG TACCTCTCTT CTGTAGAGAC TGAGGCTCTT 1320
GGGAGGACTT TTTTTTTTTT TTTTTGAGAC GGAGTCTCGT GCTGTTGCCC AGGCTAGAGT 1380
GCAGTGGCAC AATCTCGGCT CACTGCAAGC TCTGCCTCCT GGGTTCACGC 1430
|
