| Tag | Content |
|---|
EnhancerAtlas ID | HS184-25063 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr5:149491590-149492820 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Zfx | MA0146.2 | chr5:149492668-149492682 | CAGGCCTGGGCTCG | - | 6.21 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTAGTCAATA GTAGCCAATC AAATCTTGTA GCTCTACGTT AACCTTTGTA TGGAAAATGT 60
AATTGTGTTA CCCACCCGTT TCTGGCTATA TAAACCATCC TCACCTTGCC CCACACAGGG 120
AAGCACTGAT CACCATTCTC TGGTTTTCCT GTTTCCTGAC GACTACCCTC ACACTTTGCC 180
CTTGAATAAA CTTCTTTAAC TAGAAAAACA AAAACAAACA AAACAACAAC AGCTTGGACT 240
GGTGTCTCAT CTGTAACATG GGATAATAGT AGGACTCAGG TCACTGGGCT TTTGGGAGGG 300
TAAAATGAGC TAATGTGTGT GAAGCAACCA GACAGCCCTG GGGCATAGTA ACTGTTGGAT 360
AGTGGTAGTC AGATTTTTAT CAACCTTTGT CTTAGTGTGG CATCTAGCTC CATTTATCCC 420
TGGGGAAACT GAGGCCTGAT GTGGTGTAAT CCACTCAAGT TCCCATAAGG AGCAGGCCTG 480
AGACACAGGG AGCTGAGATC TTCTGACCTC CAGACAGAGG CTTTTGCACC AGCAAAGATA 540
ATCCCTGTCT GGAATGTGGG CTAGTTATTT TCTTTACAAG GCAGATCCGG GTATCACCTC 600
ATTCAACTCC TGCCACAGCT AGAAGAGAAG TCACAGGCTC TGGGTGTTTT CTGAAGCCAG 660
GATCCCTGGG ATGGTGGGCT TTGTATGGCC AGGCCTTATA GCCGTCGGGT ATTTTCCCTG 720
GTGTGGCTCA GCTGCCCCTG AGTTGGCGGC TGGGCCTGTG AGTCAGAGCT GTCCCATGGC 780
TCCATTCTTT TCCCCACTTG AAGCCACAGC CCCAGACTCC TGGAGGCAGT CCAGGGAGGC 840
CTGTGGTTCC AAAATGAGGT CCTTCCCGCA CCCACTCAAA TGAAGATGCC GTTTCCCCAG 900
CTCAGAGAGA GCAAGGGAGG GGCTAAGGAC ACACAGTGAT GGATCTGAGG CTGACATCTG 960
GTCCACCTCA AGTGAGCCAA GTACAGGACT CTGGGCCCAG GTGGGAGGGC CCTAGCACTC 1020
TGTCCCCTGC CCCCAGCAAC CCTATTGCCC CTGGCCCTGT GTTGCTGCCG GGGTCCCACA 1080
GGCCTGGGCT CGGCAGGAGA GCCTATGACT CATGCCGGCC CCACAACCCC TGAGATGCTG 1140
CAGCCGTGAG GGGTCTGGGT CCTGCCAGGT CTACACCTCT CTGCCCTCAA AGCCACAGCC 1200
TGGTCGCCAC CCTATTCCCT CCCCTGTCCT 1230
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