| Tag | Content |
|---|
EnhancerAtlas ID | HS139-44856 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr5:137840140-137841550 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr5:137840177-137840192 | TGAACTCCTGACCTC | - | 6.22 | | SOX10 | MA0442.2 | chr5:137841124-137841135 | AAAACAAAGAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_27104 | chr5:137838886-137841876 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr5 | 137840205 | 137840307 | | chr5 | 137840449 | 137841139 | | chr5 | 137841242 | 137841292 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I138503 | chr5 | 137839081 | 137841522 |
|
Enhancer Sequence | TAGAGACGGG GTTTCACCAT GTTGGTCAGG CTGGTCTTGA ACTCCTGACC TCGGGTGATC 60
CACCTGCCTT GGCCTCCTGA AGTGTTGGGT TTACAGGCGT GAGCCATGGT GCCCAGCAGA 120
ACCAGAGCTT TTCTTGACTC CCTTGTTTGG TTCTGGGCTC TTAGCTAAGC CCCAGGTAAG 180
CCTGCCAGTT TCAGGGAAGG ACTCCTGGAG ATGGCTGTAT CTGAAACAGA ATTCACCAGA 240
CAGGGTTTTA GACTTGATTT ACAGAGAACC CTTTAGGTGG TGAATTGTTT TCACCTGTTA 300
TTTCTAGTGC CTGCTATTCA GCCACATCCT CAGCAACTTG CAGCACCCAA ACTGCCACAA 360
AACAAGCAAG TAACTGTGCC CTGCTTCCCT AGCTCTAATC GGATGCTCCC ACACCACTTG 420
GCTGTTCAGT TCCTAGGTCC CCTGAGACCC AGTCCCATCA GGGCTGGACT TGGCAGGCAG 480
GAATCCCCTG GCATTCACTC AAGCTGGCAA CAAAGGAGAA GCTGGCATGA AACTTAAATT 540
CCACCTTGGC TCTCAGCCCT AAATCCACCG TGCCTGTCTG GGAGTGTCAT GGCATGCGTC 600
TTGGAGCCAG AGAACAAAAG ATGGCAAGTG CTGCAGGCCC AGACAGGCAA GGACCACAGC 660
CCATATATCC TGCACCACTG TGCTGCCTTC CAACAATTTT GTCTTCAAGA ACAGCACCTA 720
GACACGCATT AGGAGGGAAA ATTACACTTC CACCAGCACA GGCATGTTCG CCCCTTCCCA 780
GCTGGTAATT GAGTTTCGTC GTCAGAGCTA TCACCTAGAT CAGGTAAGAA AATGGGTGAA 840
AAGTACGCCA AGTGCCATTA CTGGTCAATT TTACTTAAAA CAGTTTTCTC AAACCTGGAG 900
AAAGCAAACC ATGCACCACC TTGGCTCCTC AACTAGGCTT CCTAAACTAC CAAAGAGGCT 960
CTTTAAGCAC CTCAACCTTG GGGGAAAACA AAGAAAACAA ATCCTCTTCT GCTCTGAACC 1020
TGGCCTAGGA GCCCTGCTCC TCTGGACCAG CCCCTGACCT GCTTTTGGGT GGGCTACTAC 1080
TCTCCTACCC AGTGTAAGGT ATGTAAGATG AAGGAGCGTG GGAGAGAGAG AGGGCCCAGG 1140
CCTAGTTTCT GCTATTCCAT CTGGACCATT CTATTATAGG ACTCAAAGAC AGATACAGAG 1200
AGAACTTTGG AATAAGGCCT GGGATAAAAT TTTGGTGTTA TCACTAAAGA GCTGCTACTT 1260
AACCTTCTTT TGTTCTGTTT CATCACCTGT AAAATTGGGT ACACCATCTA CCTCCATGGG 1320
ATGCTGGGTT ATGGGATAAT ATACTTAACA TACCTTAAAA AAAAAAAAAA GCAAGATTCC 1380
CTTTGGCATG CATATAGAAT GGGGGAGAAT 1410
|
