| Tag | Content |
|---|
EnhancerAtlas ID | HS105-48792 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:242100810-242102070 |
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 | CTGGCATGCT TCTTCGAGAT GAAAGTTTCC CAAGCCCAGC AAAGTGGTCA CTTGGAGTGA 60
ACTGATGTAC ATACCGGGGG CTTTAGAAAA CCTCTTGATG CTGACACACT CCCAAAGGCA 120
GTGCTGAGTT GGGCCTTCCT CCCTGGACAG CTTTATACTC CTGGACACCG TCCCCAGCAG 180
GATTAGATCT GTTCTCCAGG ATCCATTTGA CCTTGAAAAC GTGGGACAGA ATGGAAATAA 240
AAGAATTTTG AAAAGTGATC TGGTGTTCCA CAGAAGCAGG ATCAAGTCTT CACCAGCTGA 300
CTCATAACCA CCGTCATGTG CTGGAGGGGA ACTTGGGAGG GCGTCCCAGG AGGACTGACA 360
TTGGAGGTGG ATCTGCCAGG CAGGGAGGAG GGAGGGTTCC CGTGGGCAGG AAGGAGGACT 420
TCTCTCAGCC AGAAGAACAC TTGAGCCCCG TGCCTGGCTC CTAATCAGGG TCATGGCACG 480
GAGCCTTTGC TCCCCCGGCC TGGCTTAGTG GCTTTGGCAG CTGTGTCTAA GCACATCCGC 540
CCCTGCCCAT GTTCAGAATG CCCCTCTACT TGGCTTCTGG AAGTATTACA GCATTCTCTG 600
TCTGTCCTGG GCCCTTGAGA GCTTGGACAG GATACAAACC AAGGGAGGGT GGTTTTGGCA 660
ACAGTCTCTT GACAGTTATT GTTAGAGATG TCATGGCCAC AAATAGCAAA GCAGCACATT 720
TAAAACTAGA GAGCAGCCCA GATGTCCGCA TTTTACCAAG TGTCTCACTA TGGAACTTTC 780
TAGGGCAACA GTGGCTCATC ACAAATTAAT GCAGGCTACA GCATGTGAGG ATGCCCCTGC 840
CCCCGCCAAG TCCTGCAGTG GTGTGTGGAT TAGCACACCA TCTCCCCTCC TAGAGTCCCC 900
ACCTGGTTAG CATGCACCTT ATCTGGTTAT TTTGTGTCTG CTGAAATATT TAAAGAATGA 960
CTTGTTCTGA GAGAGAGTGA ACTGACAGAG GAGGGAAACT GAAGTCAAAT CAATAAACAG 1020
TCATTAAACA TCCTGCTGTA GGCAAGTCAC CATGGGGAGA CCAGACAGGG CAGCGTGGTC 1080
ACTGCCTCTG GAGGTTTATG GTTGAATAGA GGAGCACACG ATCACAGCAA GAGTGATGTA 1140
GGAGGGTGTG GAAACTGGGC AAGAGGGGCA GAGTGCTGTG GTGTGAGGGC CCCCCAGGAA 1200
TCCTAAGTGA GGGTCCCAGG ATTTCAAAGA CTTGAGGTCA GAGTGCCCCG TACCTCTCTT 1260
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