| Tag | Content |
|---|
EnhancerAtlas ID | HS030-00889 | Organism | Homo sapiens | Tissue/cell | CyT49 | Coordinate | chr1:46931570-46933280 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr1:46932182-46932192 | GCCCCGCCCC | + | 6.02 |
| | | 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 |
| GH01I046466 | chr1 | 46931725 | 46933408 |
| Enhancer Sequence | AGTCTCTGCA TTACTATTTG CTAATAGTGT GCCCTTGGCT GAGGGCTCCC CCCAAAATGC 60
TTTACCCTCT GCCCCAATGC TTGTCCTCTA GACATTCCCA GAGCAGGTTC CTTCATGCCA 120
TGCAGATTTC AGCCAAAACG CACCTCCTTA AGAAGCCATC TTTGACCACT CAGTCTCATT 180
TACCTCCCCT TCCCCTACAG TCACTGCCAC ATCACCTTGC TTTATTTTCC GTTCATTTAT 240
TTCTTGTTTC CTGTGTGTCG CCTGCCTCCT TCACTAGAGT CAAATTCCAC GGAGGCAGAG 300
ACGGGGTCGG TGTGGCTCAC AGGGGTATCT GCCGAACCCC AAACAGCGCT GGACACACAG 360
AAGGCGCTGG GAGAAGGAAG AGGCCTCTCT GAACCTGTTC CCTCACCTGG AAAGTGGGGC 420
TAATCACATA ACCCTGCAGT CTCTGAGGTG GTTGTGAGGG GGATTCAGAG AGGGGACCCG 480
GGGAGCTCTG AGCGCAGTGC CAGGCCCGGA CGTGGTCACC GCCTTGTCAC TTGCGCATTT 540
CATGCTCTGG CCTCCCAGGC CGGGCGATGC GGCCGCGGGG CTGCAGCTCC CGGCGAGGCC 600
CGCCAGGCCC CCGCCCCGCC CCGCCCTCCT CGGGCCCCGC TCCTTCCCAG GCGCCCCCGC 660
GCCGCCGGCG CTTTGAAGTC CCAATCCGGC AAATAGAGTC AATCAATTAT GAAGGGAACA 720
ATCTGGCGGC CCCTCGGGGA GCGGCGGCCG AGCGATCCCG GGGGATTAGG CCGCAAATCG 780
CGCTGAGCCT CCCTAAGTGA CAGCGAGAGA ATCGCGCGCG GCGGCGACGG CGGCGGCGGG 840
AGCGGGAGGG AGCGCGGCCG CTAACCCGAT TATGCAGATC CGCGGGGGGC GCGGATTAGG 900
CCTCGGGGGC GGCTTCGCCC TAAGCGGCTC TCGGATTTGG GAAAAGTTTA CTCGGGCGGA 960
GGGGGCGGAG ACTCCCCCGG GCGGGCGGCC GGGACTTCTC CCAGCCGGGT GAATGGAGGA 1020
CCCGCCTGCA GGAGCAGCCG CGAAAGAGTG GAGCGGGCGC GCCTGCTGAG CCACAGCCAC 1080
AGCAACACTT TGCAGGCGTG CACACTCACA CGCACACCCA GGCCACAACA GCCGTGTCTG 1140
CACCAGCCCA CGGGCGCACG CGCGCTGCCC ACGATCACCC TCCCAAGCCA CAAAACACTC 1200
GCGAACGTGC GAGGCCGCAC CAGCCCACAT AGCCAGACCC ACGCCGGCTC ACACGCGCAC 1260
GCAGCACTGC CTCGTGCTCA CACAAGCATG CACGTACTCA CAGACACGCA ATTTGATGTT 1320
CGGATACCTG CCTCCTGTGG TTCCAGCAGA ATCCCTCAGT GACACAAGGT GTCCCTGCCA 1380
GCCTATGTAG ACGTAGGACT GGTGCACGGC CCTGCACCTG TGCTCTCCCA CGGACCTCCC 1440
TGCAGCTCCT CTCCTCTGAA GGACCTTGAG GACAAGTGTG TGTTAGTGTC TGTGAGTGTG 1500
TGTGTGTGTT TGAGCGTGGC CTGTCTCTGG AGTCTGGGCC CAGTTTTGGC TTCTGCAACT 1560
GGGGCCTTCT CAGGGTAGGT GGAAAAGACT GAGGCAGGAC GCTGGGATGG AAACAGGCCG 1620
AGTCCTCTTG GTGACTCTGG CTAAGGGGTC CTCTCCGCAG GGCTGGGGAT CCAAGACATT 1680
CCTCACCAGG CCCCTCTGGG CCAGCCCCTT 1710
|
| |
|
|
|
