| Tag | Content |
|---|
EnhancerAtlas ID | HS118-04011 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr11:125794560-125796170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr11:125795172-125795185 | GGCAGCTGTTCCC | + | 6.24 | | RREB1 | MA0073.1 | chr11:125795871-125795891 | ATGGGGGTGGTGGGTGGTGG | - | 6.26 | | RREB1 | MA0073.1 | chr11:125795868-125795888 | GTGATGGGGGTGGTGGGTGG | - | 6.3 |
|
| | 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 |
| GH11I125925 | chr11 | 125795038 | 125795806 |
|
Enhancer Sequence | ACAGATTTCC TTCCCCATGC AGATGAAAGC AGACTCTCCG AGGGCAGAGC CCAGAAATAC 60
CCACTTCCAT AAGGGAGCCG CAAGTGCAGG TAGAGCAGTG GTAACGAAGA TGGCCGTCCC 120
AGCGGGAGAC CCTCAGGCAG AGAGGCCCTT GGGGACAGAA CTTGTAACAC ATGGAACTCC 180
TGCTGCTCGG TGTCCATCCT GGTTCTCCTT ATCCTACATC TGCCCTTCTC TCTGGACTGG 240
AAGCTGGTGA TCACTCTTGT CCACTCAATA CCCCTAACAC AGTGCCCAGT GCATTCTAAG 300
TGCCCAAGGA ACCTTTGTCT TTGTTGAGTA AATTTTTTTT TCTTTTGCCA CTTCCTCATT 360
CACTAATAAT TTTTTTTTAG GTTTTCCATC CTAGTTTTGA ACCCCAATTA CATGGCACAG 420
GATGAATGAG CATGAGAAGT GTATCCAGAT ACTTTGTTCT CTTACTATTC GAGAATCGAG 480
TTGGACCTTC CACCGTGCTC AGCTCCGCCT TGGGGTGTCC TAAATAAAAC TTTACCACTT 540
TCCTTTACAG TTCAAATCTC TGGTAAGATC TCCGCCAGTT ACCCTCACAA ATGTCCTCAG 600
TAATTTTTGT TTGGCAGCTG TTCCCACAGG TCTGCATGAA CCAGGTATTT TTCTGCGTTC 660
CCTTTTGCCC CCTCCTCACG TCCCTTTGTC TCACCACCTA GGAGGCAGCA AAGCCATCCT 720
GTGTCACAGC TGCATTAACA CGAACTGGCT AGTTTGGTGA GTCAACAATC CAAAGGCTGT 780
TTTTTGCAGG GTGCAGCTCC TGTCAGAGCT GTAAGCAATT TTCCCGTCTT CCTGCATGGC 840
CTGGCCAAGG TCATCTCTCT CAGTGCCTGC CTGAGGACAG AGTAGATAGA GAGGCAAGGA 900
AACACCAGGT GATTTCAGTG CAACTGTGAG CTGGGTTCAT CAGCTGTATG TTTCTTGGCA 960
CCAAATACTA AACCAAATCC GTTAAGTTTA TCTTGGCCAG CTTAATACTG TTAGCATATT 1020
GAAATTCATG ATTACGTAGA GCAGGACTGT GATTTCCAGT GGGTAAGTGA ACACCTCGCA 1080
TGGAACACGG CTGCTATGAT GTTAGGTGCT GGATCTAAGG CAACCATTAA TAATAGGAAA 1140
GGCAAATAAG TTGGTCATAG TCTGGTAGGA TGTGTGACAG CCGCTTTTCA AGAGACATTA 1200
TTGCTTTTGG TCATGAGAAA GTGTTGATCC TCCTCAGCAA AGCTCGGTCA CCATGAAAGC 1260
TGCTGGCAGT CTCTGCACAT ATGACCAACA GTGGAAAATC TTAGAGGAGT GATGGGGGTG 1320
GTGGGTGGTG GGCAGTACCT TTCCAGACAG CAGAGAGAGA GAGGCTGGTT TTGTCAAGCC 1380
TTGGCTTGGT TCCTGGTCCT CTGAGAGGCT CAGTCTCCTT CCTTTTGATT CAAGGCAGGA 1440
CCTAGATTAG AAAGAGAACC CCTGCAGAGA CAGTCCAGCT GTTGGGATGG GCCTGCACTT 1500
TGCTCTCTGA ACCGGGGGGC ATTACTATGT TCTCACCCAC ATTGTACAGA CAGCCCATCA 1560
TGCTCAGCCT TGCAGGAGGG TCTTCAGGAG CCCAGCCATC TGGCACATAC 1610
|
