| Tag | Content |
|---|
EnhancerAtlas ID | HS098-47315 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:179340430-179341860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr5:179341625-179341645 | CCTGTGGGGGTGTTTTGGGG | - | 8.67 | | ZNF263 | MA0528.1 | chr5:179341641-179341662 | GGGGGAGGGAGGAGGAAGGAG | + | 6.51 | | ZNF263 | MA0528.1 | chr5:179341645-179341666 | GAGGGAGGAGGAAGGAGGAGA | + | 7.41 |
|
| | 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 |
| GH05I179913 | chr5 | 179340179 | 179341921 |
|
Enhancer Sequence | CCTTCAGCTT AGGGTGGAAA AGGAAGGAAA ACCCAAGATG AGTGCAGGTG ACGACCGGGC 60
GGCCCCCACA GGGTCTCTGC AGGACCACAG GAGCCAAGAC TCAGGCATAA GAGCATCACC 120
CTTTCAGCAG CCAAGGCGGG TGGCACCTTC CCCTCCATGG TCACTGGAGG CTGTGGGGCC 180
ATAGCTGCAG AGAACGCAGG CGGCGGGAGA CCCTCTCAGC CTCTCTTCTT CCAAGCTCAG 240
TTTCTTGAGA TCTTCCAGGA TACCCACAAA AAAGAGGGTG AACCTTTAAC AATGCCCCAG 300
AGGAGCTTCG TGGCTACAGG GGGCCTCCTG ACCCCCAACC CAGCCCTCTC AGCCAGGCCT 360
CAGGAGGCTA GTGTGACCTC AAAACTCAGA GCCCCCGTGA GACACAGGGC CAGCCAGTCC 420
CATGCCTTGC AAAGGGGAAC GTTCCTCCCA GGTGTGGATT TGGGGGCTCA CGCTTTGCTT 480
TCCCTGTAGT TGCCTCGGAC AGTAAGGAAA GGAATTCCAA GGAGCAGACA TAGGCACCTT 540
GTCCCCACCT GCCTTCTTCC GGTGTTTTTT TCTGATGCTA CAATACTTCA AACACACAGG 600
GCTTCTCCCA GTCCTTCTGC AAGGCTCTTA ACCATAGCCC AGGGAGCTGT GTGAATATTA 660
CAATCAACAG CCTTTCCTAA TGGGCTGAAA GGAGGGTGTG TCGAAGCTTT GGAATGCTTT 720
ACCAACAAGG CCAAAATACA AGACAAAACT CCACGCCCCT CATATGTAAC AACTGCCCTA 780
ACCAGACCTG GGAGGGGAAG GTGCCTATTT TAAGCTGTGG GTATCGCCCT GCGATGAGTC 840
CTTACTCATC TTCCCACACT CCCTGACAGT GTGAGCCAAT GTTGACTTTA GTCACATTAA 900
ACTCTGCTTC CGGGTGACAC TGAACACACG AGAGGAAGTG AGAGCTAGTT GGACAGCCTT 960
TCTTGAAGAA GGAAATCATA CTCAATTGCT TTTCTAAATC CATTGCCTTC AGTAGCTCCT 1020
TCTGTCCACA CTTTAAATGT CAGTGTCCCC AGGGCTTTAT CCCAAGCCCC ATCCTCATGT 1080
CACTGGGTGG TCCCAGCCCC ACTCTGGCTT CCACCTCCAT CTGAACTCAG GGACACCTCT 1140
CCTGGCCAGC TCCCCTTGGG AGATTCTGCC TCCAGCGCAT GGGAGGGTAT GCATGCCTGT 1200
GGGGGTGTTT TGGGGGAGGG AGGAGGAAGG AGGAGATTTG GGTGACATAG ATATTGTGAT 1260
TACATGGAGA TACTTCAGCA GGACAAGATG GTATGTCCAC TTAAAAACAC AGCTTCTGAC 1320
CGGGCGTGGT GGCTCATACC TGTAATCCCA GCACTTTGAG ACACTAAGGC GGGAGGGTCA 1380
CTGGAGCCCA GGAGTTTGAG GCTAGCCTGG GCAACATGGA GAAGCTCTGT 1430
|
