| Tag | Content |
|---|
EnhancerAtlas ID | HS052-22846 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr2:242100790-242102170 |
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 | CTTGATCATG GTCATCTTCT CTGGCATGCT TCTTCGAGAT GAAAGTTTCC CAAGCCCAGC 60
AAAGTGGTCA CTTGGAGTGA ACTGATGTAC ATACCGGGGG CTTTAGAAAA CCTCTTGATG 120
CTGACACACT CCCAAAGGCA GTGCTGAGTT GGGCCTTCCT CCCTGGACAG CTTTATACTC 180
CTGGACACCG TCCCCAGCAG GATTAGATCT GTTCTCCAGG ATCCATTTGA CCTTGAAAAC 240
GTGGGACAGA ATGGAAATAA AAGAATTTTG AAAAGTGATC TGGTGTTCCA CAGAAGCAGG 300
ATCAAGTCTT CACCAGCTGA CTCATAACCA CCGTCATGTG CTGGAGGGGA ACTTGGGAGG 360
GCGTCCCAGG AGGACTGACA TTGGAGGTGG ATCTGCCAGG CAGGGAGGAG GGAGGGTTCC 420
CGTGGGCAGG AAGGAGGACT TCTCTCAGCC AGAAGAACAC TTGAGCCCCG TGCCTGGCTC 480
CTAATCAGGG TCATGGCACG GAGCCTTTGC TCCCCCGGCC TGGCTTAGTG GCTTTGGCAG 540
CTGTGTCTAA GCACATCCGC CCCTGCCCAT GTTCAGAATG CCCCTCTACT TGGCTTCTGG 600
AAGTATTACA GCATTCTCTG TCTGTCCTGG GCCCTTGAGA GCTTGGACAG GATACAAACC 660
AAGGGAGGGT GGTTTTGGCA ACAGTCTCTT GACAGTTATT GTTAGAGATG TCATGGCCAC 720
AAATAGCAAA GCAGCACATT TAAAACTAGA GAGCAGCCCA GATGTCCGCA TTTTACCAAG 780
TGTCTCACTA TGGAACTTTC TAGGGCAACA GTGGCTCATC ACAAATTAAT GCAGGCTACA 840
GCATGTGAGG ATGCCCCTGC CCCCGCCAAG TCCTGCAGTG GTGTGTGGAT TAGCACACCA 900
TCTCCCCTCC TAGAGTCCCC ACCTGGTTAG CATGCACCTT ATCTGGTTAT TTTGTGTCTG 960
CTGAAATATT TAAAGAATGA CTTGTTCTGA GAGAGAGTGA ACTGACAGAG GAGGGAAACT 1020
GAAGTCAAAT CAATAAACAG TCATTAAACA TCCTGCTGTA GGCAAGTCAC CATGGGGAGA 1080
CCAGACAGGG CAGCGTGGTC ACTGCCTCTG GAGGTTTATG GTTGAATAGA GGAGCACACG 1140
ATCACAGCAA GAGTGATGTA GGAGGGTGTG GAAACTGGGC AAGAGGGGCA GAGTGCTGTG 1200
GTGTGAGGGC CCCCCAGGAA TCCTAAGTGA GGGTCCCAGG ATTTCAAAGA CTTGAGGTCA 1260
GAGTGCCCCG TACCTCTCTT CTGTAGAGAC TGAGGCTCTT GGGAGGACTT TTTTTTTTTT 1320
TTTTTGAGAC GGAGTCTCGT GCTGTTGCCC AGGCTAGAGT GCAGTGGCAC AATCTCGGCT 1380
|
