| Tag | Content |
|---|
EnhancerAtlas ID | HS184-19033 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr21:42518730-42519880 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BARHL2 | MA0635.1 | chr21:42519109-42519119 | ACCGTTTAGC | - | 6.02 | | KLF4 | MA0039.3 | chr21:42519726-42519737 | GCAGGGTGTGG | - | 6.62 | | Pou2f3 | MA0627.1 | chr21:42519657-42519673 | TCTAATTAGCATAATA | - | 6.93 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATAAAAGCAT CCAGATTCTA CCATTTTCAA GGGACTGTTG CAAAGATCCA AGGGCACCGT 60
GAGGCTGCAA ACCTCCTTGA ACTCTGAAAA GCAATTCACG TATTAGTTGT GGCTGATATT 120
ATGATGAGTG CAAGCTGCAG GCAGCAGCGT GGCCAGCCCT GAGTCCACCA GAGGGAGACG 180
AATCACACCA CTGGAGGCTC AGGGGAGACA TCAGCTGTGA GGGGGCAGCA GGATGATTGC 240
CATGAAAGGG AGGACAATGG AAGAGAAGGG AGGAGATGGA CATGGGGTTG GGAGAGCCAC 300
AGGGACAGAG AGCATGGAGA GCCCCAAGCA GAGAGTGGCA GAGGGGCACT CAGAGACACC 360
CTCACCGCCC CTGGTGGATA CCGTTTAGCT CCCTCAAAAG ACGAGGAGCG CTTGAGCAGG 420
GAAGGGGAGC CCCCAGAAGC ATCCAGCCCA GCACTGGTCG GGAACTGGAA CCAGCCGCTG 480
AGGCTCCCGT TCTACCCCAG GGCACTGACA AGTCACGAGG CTGCAAATCC TAGGTATTTA 540
CCCACCTCAC TTCCTGGTCT TTAAGATTGC AGCTGCCAAA ACCTTGTCAT CGTCCTACGA 600
TTGTTTTCAG GGGTTTCAGC TCGACTACTT TAATGCAATG ACAGTGTCAC ATTTATATCC 660
TGGAACCCAT CCAGATGCTC TGGAGGCCAG AACACCCTGC CAGGAGAGGA TAATGAAGCA 720
GATGACACCT AAGAGGGTTG CAGGCCCAGC TGACAACCCC CTACCCCAGC CTGAGTTGGC 780
AACCTTTGGA CATAGTCCTC AGCTTGGGGG CAGAAGAGGC TGCTGGGGCC CCCTGAGGTG 840
CTGTTGTCTT CTGAAAGCTT CCTCATTCTG GTTGTGCTGA GCAGGGAGGT CAAAGCCTCT 900
TACTCCAAAA AGTCAGCAGA TCATTAGTCT AATTAGCATA ATAAAGCTGG CATTTTCGCT 960
TGGCTCTGAG CCTGGAGTTA AGTAGCTTAC AGTTGTGCAG GGTGTGGACT GCACAACCCA 1020
ACGGTTCTCA TTCCCATGGA CTTGCTAGAC ATGGCACCCC CCAGAGGCTG TTCAGTGTCC 1080
AGCTTGTTTA ACCCTGAGCA GGGTCTGGAA GTTAGGGACC TACAGGCTAT GGTGGTGTAG 1140
GGAGGAAAAT 1150
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