| Tag | Content |
|---|
EnhancerAtlas ID | HS108-33505 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr5:179519950-179521430 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr5:179520724-179520738 | TTCCTTTCATGTTT | - | 6.07 |
| | | 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 |
| GH05I180093 | chr5 | 179520615 | 179521430 |
| Enhancer Sequence | TTACCCCTTG CACTCGTTTT GCTGGGAAGG GGGTCCGTAG GTTTCCCTCG GCTCCTCTCC 60
TCTGCCTGCC CTTTGAGATT CCTGCTCCTG ATGCTTGGCA AATACCCTTC ATCCTCACGG 120
CCCTGAGGAG CTCCCCGGCT CTCCCTCCCT GGGCCTGGGC CCCAGGGTGT TTCCTCCTCT 180
GGTAGCTGCG TGTGTCTGAG ATGCTATTAT TTTGGAGGAA CATCACATTT GAGAGAGACC 240
CACCTTTTGC TGTCTGTGTA CTCCCCTTCC CTGTTTTCCT GCTCATTTCT TTGGGTGCAG 300
AGCTCTCTTG CTAGGCCATA GGCCCTCTCA GCTTTGGGAG CTCTACCCTA CTCCCTACAG 360
TGATTTACTG TACTTTTTGG TTGTAAAATG TTTTTCTGGG GGGATGGGAG ACAGGGTCTC 420
ATTCTATCAC TCAGGCTGGA GGGCAGTGGC TCAATTATAG CTCGCCGCAG CCTTGAACTC 480
CTGGGCTCAA GCTATTCCCC TCCCTCGGCC TCCCAAGTAG CTGGGACTAC AGGTGTGCGC 540
CACTACGCCT GGCTAATTTT TAAATTTTTT GTAGAGACAA GGTCTCCCTA TGTTGCCCAG 600
GCTGGTCTTG AACGCCTGGC CTCAAGTTAT CCTCCTGCCT CCCAAAGTGC TGGAACTGCA 660
GGCATGAGCC ACCATGCCCA GCTTAAAATC CATTTAAAAA AAATCAAAGT AGTACTTAAA 720
GGTAATTTAT AGTGTTAAGA GGCTTTTAAC AGAAGCTGCC ATTCCCACTC CCCCTTCCTT 780
TCATGTTTTC TGTTCCGCAG AGGCGTTTGG GCTTCTCCTG GAGCCCTGTC CTCCCACTGG 840
CTGTCATCTG CTGGGTGCTG ATAAGAGGCT GTCTCCCAGG ACTTCCTGTT CTCTCCCTGC 900
GTTGGGTCCT GTGACTGCTG ACCCACATCA TCTTTCTTGG TTTATTTCCT CATTTTGGTG 960
GCATATGTCT TGCTGCAGGA ACATAATCCT GATGCTAAGC GTTGGCAAGG ATTTGTGGGG 1020
CCACTTAACC ATGCTGGTGG GCTGGTACGT CCATTGTGGG GTGAGGGTGC CTTTCCACGT 1080
CAGTACATGA AGCATCCTTA TTACAGCTGC AGAGTATTCA ATGGGGAGGC ACACAGGGAT 1140
GTGTTTTCCT GGCTTCCTAT TTATGGACAA GGGTTGTTTC CAATCTTTTG CTGTCAAACA 1200
CTGCTGTGAC GAATAGCCAT ATGCAGACTT CATTTGAAGG TGTGTAAGGG TGAAGGGAAG 1260
ATTACTTGCT GGAGGTGACA TTGCCATGTC ACAGCATCCA CATATTTGTA ATTTGTTGTT 1320
GTTGTTTTGA GACGAAGTCT TGCTCTTGTT TCCCAGGCTG GAATACAGTG GCACGATCTC 1380
AGCTCACTGC AACCTCTGCC CCCAGGGTTC AAGTGATTCT CCTGCCTCAG CCTCCCGAAT 1440
AGCTGGGATT ACAGGCATGC GCCACCACAC AAGGCTAATT 1480
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