| Tag | Content |
|---|
EnhancerAtlas ID | HS088-09710 |
Organism | Homo sapiens |
Tissue/cell | HeLa-S3 |
Coordinate | chr11:47442280-47444120 |
Target genes | | Number: 36 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr11:47443583-47443604 | TTTTTGTTTTGTTTTCTTTTT | + | 6 | | MEF2A | MA0052.3 | chr11:47443374-47443386 | TCTATTTTTAGT | - | 6.27 | | MEF2B | MA0660.1 | chr11:47443374-47443386 | TCTATTTTTAGT | - | 6.32 | | MEF2C | MA0497.1 | chr11:47443373-47443388 | TTCTATTTTTAGTAG | - | 6.57 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 47442892 | 47443115 | | chr11 | 47443634 | 47443732 | | chr11 | 47443434 | 47443590 |
|
Enhancer Sequence | AGGGCACAGG AAGCCCGAGA TGCTGGTGAG GGCACAGCTT AGGCAGAGCC CTCCCCTCCT 60
CTACCCCCTG GAAGCCTAAC CTAACCCGTC CAGGGCAGGG AAATGGCTCA CTCAACTTGG 120
GGCCCCCAGC CCAGGGACTG GCACATAAAA AGTGTCATTA ATTGTTGACC ACATTCAGAG 180
ACTGAAGAGA CTCCTAGAAT CAGGTGCTGG GCTGAGGATA AAACAGTGAG CAAGGCTGGG 240
TGTGGTGGCT CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CAAGGTGGGC CTATCACCTG 300
AGGTCAGGAG TTCGAGACCA GCCTGGCCAA CCAGGTGAGA TGGTGAAACC CCATCTCTAC 360
TAAAAATACA AAAATTAGCC AGGCGTGGTG GCAGCCACCT GTAATCTCAG CTACTCGGGA 420
CACTGAGGCA GAATTACTTG AACCCGGGAG GTGGAGGTTG CAGTGAGCCG AGATCACGCC 480
ACTGCACTCC AGCCTGGACG ACAGAGCGAG ACTCCATCTC AAAAAAAAAA AAAAAAAAAA 540
AAAAAAGCAA AACCAACCAC TGCTTGGGCT GTTAACTGTG ATGAATGTAC ACTTGCAAAC 600
TGAGCTAACG CTTAAAAACA CAGGTATCTG GCCCAGCCTT GGACGGTGCT GTACAGGAGA 660
GCCCAGGCAG GCATCCCCCG GGAAGTATCC CTGAGGCTGA GATCTGAAGG TTGAAAGCAC 720
ACCAGCTAGG CAACCAACCA GTGGAGAACA GGGTAAGAGC CACGGCGGGC CTGAAACGCA 780
GGAAGCACCG TGGCAGGAGT CCAGAGCAGG GGAGGCTGGG GACAGGCATG AGATGAGGGT 840
GAAGGCGCAA AAAGGCAGCA CACGTTGAGC CTTGTAATTC CAGCATTTAT CCCAGGGAGC 900
AACAGGGAGG CCCAGGAAAG TTTGATTTTT TTTTTTTTTT TGAAACAGAG GCTCACTCTG 960
TCATCCAGGC CGGAGCACAG TGGCACAATC TCAGCCCACT GCAACCTCCG CCTCCCAAGT 1020
TCAAGTGATT CTCCTGCCTC AGCCTCCCAA GTAGCTGGAA TTACAGGCGC ACACCACCAC 1080
ACCCGGCTAA TTTTTCTATT TTTAGTAGAG ATGTGTTTCA CCATGTTGGC CAGGCTGGTC 1140
TCGAATTCCT GACCTCAAGT GATCTGCCCA CCTCAGCCTT CCAAAGTGTA GGGAATACAG 1200
GAGTGAGCCA CTGCACCCAG CCAGGGTTTT TAACAGGATT GGTTTATGTC AGGGACCACT 1260
GTGGGTTCAT GTGAGCGAGG TGGCCAGATT CCTGCTTTGG CTTTTTTTGT TTTGTTTTCT 1320
TTTTTTTTTT TTGAGACAGA GTCTCACTCT TTCACCAGGC TGGAGTGCAG TGGCGCAATC 1380
TTGGCTCACT CCAATCTCTG CCTCCCAGGT TCAAGTGATT CTTGTGCCTC AGCCTCCCAG 1440
GCATCTGGGA CTACAGGCGC CTGCTACCAC GCCCAGCTAA TTTTTTGTAT TTTTAGTAGA 1500
GACAGGGTTT CACCATGTTA GCCAGGATGG TCTCGATCTC CTGACCTCGT GATCCGCCTG 1560
CCTCGGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA CCGTGCCCGG CCCAGATTCC 1620
TGTTTTGAAA GGAACATGCT GGCAGCTGTG GGAATGAATG GCTGGGGAAA CAGGGAGGCT 1680
ATTGATCAGG AGTTAGGAAT TGGAATCTCA AGAGTTGAGG AGCCACCATC CAGGGGCAGG 1740
AGGGGATACA GGGTGGGAAG GAACCACAAT TTAGCACAAC TGAGAGTCAA CCCGCTTCCC 1800
CTTACCGCCA CAGAGATCGC TAGGGACCCT TGGCCCTCCC 1840
|
