| Tag | Content |
|---|
EnhancerAtlas ID | HS184-00437 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr1:27625580-27626680 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF143 | MA0088.2 | chr1:27626195-27626211 | CAGTGCATGATGGGCA | - | 6.15 |
| | | 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 |
| GH01I027298 | chr1 | 27624550 | 27628566 |
| Enhancer Sequence | GTTGGGTAGA ACTCAGTGGT CCTCATCCAG GCTGTAGGCT AAGAGCTCAG CTTCACTCCT 60
GCATTCTTGC TAAGAGAGGT TGGTGATTTC CTAATCCATA TGTGCCCTCA GCATGTTCTC 120
TGAGCTCCTA CTATGTGCTA GGTACTAGGA ACACAAAGTT CTATCACTCT GAGTTCCTGT 180
GCTCCAGAGG AGCCTCTCCA GACAGTGGGT AAAGTGGTGG ACATAGTTCA GCATTAAAGA 240
GATAGGAAGC AGTGAGTCTT GTGAATGGTC AGGTAAAGGG CTGTGGGCAT CAAGAAAAGT 300
TGGGTCGCTT TAGCTGGGGA GCAGGGAAGC ATCAGAAAGA CATGGCGTCT GAATGGGCTT 360
TAAGTGTAGG CAGGCTTAGA CAGGAGATGA AGGAGAGGAG GGGCCTGTGG GGGAAGGACA 420
TTCCAGGGAG ATGAAATGGT GTGAACAAAG GCATGGGGGT GGGGGACTGA CTGAAGAGCT 480
TGTTTGCAGA ACAGCAAATC CATTTGGCTG GAGCAGAGGG TTCGGAAAGG GACTGGCAGG 540
AGATGAGTCT GTGAGGTAGC CTGGGGCCGG CCTAGGGAGA GCTTGGAATG CAGAGCGGTG 600
ACGTTGGCCT CGATTCAGTG CATGATGGGC AGCTACTGGA GAGTTCTGAG CAGGAGAGGG 660
ATGTGCCGAG GGCTGTCCTT TCAGGGAGAT TGATCTGGCA GTGAGTCTAG GAAGGGTGAG 720
CCCTGGGGCC AGCCTGCTCT CTACCCCCAT CCCCACATGC CTGCCAGTGA CCCCTAGAAT 780
GTCACATTCT GTCCTGGGCC AGTCTCCCCA GGGCTGCCAT CTGCTCCTGG ATGCAGTGGG 840
AGCTGTCACC CTCTGGCTCC TGGCTGGTCT CTGGTCTGGC TCTCCCCAGG AGCTCAGAGG 900
GGCACCTTGC AGGCAGTAAT TGGGTTTCCA AACAGTGCCT GCTCCTTCGT CAGAGCCACT 960
CATCCTGACG CAGGCCACGC CATTGAAGCA GCTCTGTTTC CTGCCTGCCC CCACATGGGC 1020
TGAGCTGCTG GTTCCTGGTC TGAGCGTGGC TGTTCCGAGG ACTGGGTGCT CCCTCTGAGT 1080
GCTGCAGAAG GAGGCTCAGG 1100
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