| Tag | Content |
|---|
EnhancerAtlas ID | HS030-00218 | Organism | Homo sapiens | Tissue/cell | CyT49 | Coordinate | chr1:11399350-11400830 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LBX2 | MA0699.1 | chr1:11399704-11399714 | GCTAATTGGC | - | 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 |
| GH01I011339 | chr1 | 11399268 | 11400731 |
| Enhancer Sequence | TGAACAATGA GACAGCGTGG GGGTGAGACG GGAGGACACA CCGGGAGGGG CGCAAGAAAT 60
GCCAGAGGCA GGAGACAGAT GGGTCCAAGG GCCAGAGAGC CTGCTCCAGT GGCTCCTCGG 120
AGTGAGATGG GTCAGAGAGG GAGGCAGGAG ACCAGAAAAT ACCAAGGAAG AAAAATCTAA 180
GGTAAGGGAG ACCAAGAAAG AAAGAAGAAG GAGTCAGACG TGCAGCTGCA GGGACAAAGA 240
CACATAAACC GGGGGTGAGA GAGACAGAGT GAGAGTTGCC TCCAGCTGGG GCTGGGTGGG 300
GAACTTAGTT CCCACCAGGG TTGTGGACTT GGGAGCTTGC TTGCGGGGAG GAGGGCTAAT 360
TGGCGATTTC ATCCAGGTCC TCCAGAACGT CTGCAGAAAA ACAAACCCGC TAAACATCTC 420
TCACCGTCTG TCATCTTCAT TTTGCTTTTG TCTTCAGAAT AAAGAGAATC TGAAACTCCC 480
TAGGAGAAGC GGCTCCAGCG GCTCTCAGGC TGTCTCCCGT TCTGCTCCTT CTTCATGCTT 540
TTCTGGTTGG AGTCTTTGTT CCGCAGCTTC TTGCCCTGGT TCAGGCTGGC GGCTGCTCTG 600
ACCCGGCGTG CTGGGGTCTC CATCCCCATC TCTGTCACAC TGTGGTCTGG AGTGTCTGGG 660
TCTCTTGCTC CCCTCCCCCT CCCCCCAGGC TCAGCCTGAG CCACCCCACC CCCCTTGGCC 720
CGCGTGGCCG CTGCTGATCC TTGCTACTCC CAGCTGTCTC CGTGGCTCAG CCTGCAGATT 780
GACAGGGCCC ATAAATCACC GTGGCAAGGC AGGGCCCTGG GAAAGGAACA CGGGGCCAGG 840
TGCTGACAGG GCTGGCCTTG GGAGCTGGGG CTTTCGGCTT TCTGGTGAAT CGCTGGGGCG 900
TGGAGCCTGT GGCTTCTCTC CCAGCTAAAT GGAGCATTTT GGTTGCAGTG CCTGTGTCTC 960
CTGCCGATTT TCTCCAGCTC CCTGGAAGGT GGGACAAGAA GAAATAGGTT GAATGTGAAG 1020
CAAGTGGGAT TCGGGTTAGA CTGAAAAGAA GAATTTGCAG TGATGAGGCT TAACTTTGGA 1080
AAGAGGAAAC ACTGGGATGG GAAATGGTGA AACCCCTTGG CAAGGAGTTG GTAAAATCTG 1140
GATGGATTCT GTCTGATGAT TTATAGTGCT GCCTGGAGAC AGGGGAATGA AACATATGAT 1200
CCACTCGACA CAGAAGCCTT TGCTTTGTTT GAGGGGAGCC CGGGGGCCAG GAGAGCAAAG 1260
AAGTTACCAG TGGGGGCTTG GGGAACATGC AGCTCCCCTC CTGACCTGCT GTGTGATCCT 1320
GAGCAAGTGA CTCAACCTGG CTGGTCTCTA TCTGTAAAAT GGGGATAGTC CCACTTCGTA 1380
GACTTACCAT GAAGCTTAAA GGGCAGTGTA TGCAAAGGGC TCTGCACAGT GCTTGGCACA 1440
GAGAACTTTT AATAAAGCAC AGTTATAGGC CAGGCATGGT 1480
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