| Tag | Content |
|---|
EnhancerAtlas ID | HS052-24119 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr21:30374680-30376060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr21:30375507-30375527 | GCTGGGGGGGTGGGGTGGGG | - | 7.81 | | Zfx | MA0146.2 | chr21:30375682-30375696 | GAGGCCGAGGCGGG | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH21I029002 | chr21 | 30374436 | 30376321 |
|
Enhancer Sequence | ACAAGGGAAA GCAGGTTTAC AAAATCTGAA AAGCCAAATG CCCCAGTGGG GAAAAAACCC 60
TCCATTTCGG TAATTCCCTG GTTAAAATCG AGGAACACCC TGGACTTCGA AGGCACCACC 120
TGGGTCCCAG GGTGCACCAT TCCTCTAATC CCCCAGTTGC AGCAACATCT GGGAAGTCCC 180
GAGAATGGGG ATCTATGCCT GTTTTTCCAA AAGATAATAA GCGTCAACAA CAACAAAAAA 240
ATAAAAAGTC CAACTCCGCC CCAAAGCAGC ATCTGGCTGG CCTGCGAGAT GCCCACTGGG 300
GAGGCGAGTC CGCAGCTTAG GACTCAAGCC CGGGGTCGGA AGCTATTGCC GAAATCCGAA 360
ACGCAGCGCT CGCAGCTGCA GTGACGCGAC CTGCTCATAA GTCCCCGTGC TCACAGCATC 420
CCGGCAACTT ACGAGCTAGT GCTTCCGGGT CACCCCGGCC CAGGAAGGCG CACGCGCGAA 480
GCATAGCGAG CTTCACTCCG CACTCTTAGG CTGCGTGTGA GGCCTGCGAG TGCTCGGGAG 540
CTGCCGCGGT CACAAGAGAA AGCCTAGCTG TCAATGACAG CCCCAGAGCA TCTGGGCGCC 600
TTGCGATACC CGGGTGTCTG TAGGCAGCCA GGAGACACTT CCAAGCTGAT CTGGAATCTT 660
TCCTCGCCCA GCTCTGTCCC TCGCAGGGAT GGCAAAGGAC ATTACGACCT ACATCCCTTC 720
CCGGATCTGA TGGCTTCAGA TTGGCAGATT GTGTTAAAGT GGAAGGCTCG TGGTGCCCCT 780
TTGCTGAGTT TTTATGGACT TAGTTTTCCC AAGTAGTTCT AATTATCGCT GGGGGGGTGG 840
GGTGGGGCGG GAACGTAATT TCTGCGTCTG CCCTTAAATA CCTTTAAACC TTGGCTGCAT 900
TGCCGCTTTT ATGGAATTTC ACCCATAGTC TGTCTTTTTT AGTTTCCCTG ATACGCATCT 960
TTCTTAATAA TAATAATAAT AAATAAATAA ATAGCACTTT GGGAGGCCGA GGCGGGCGGA 1020
TTACCTGAGG TCGGGAGTTC AAGAGCAGCC AGGCTAACAT GGTGAAACCT ACCTCTCTAC 1080
TAAAAATACA AAAATTAGCG GGGTGCAGTG GCGCGCGCCT GCAATCCCAG CTACTCCGGA 1140
GGCTGAGGAA GAATTGCTTG AACCTGGGAG GCAGAGGTTG TGGTGAGCCT AGATCACGCC 1200
ACCGCACTCG CACTCCAGCC TGGGCTACAG AGCGAGACTT CGTCTTAAAA AAAAAAAAAA 1260
AAAAAAAAAA AAAAAAAAAA AACAAGGCAT GTGGCCAGTA TTCCCTGCCT ATACTTGTTT 1320
TCTTTAGAAA AATGTAACTT TTAAACATAA TTTGACTTGA AACGGTTTCT TTCCAGGATT 1380
|
