| Tag | Content |
|---|
EnhancerAtlas ID | HS184-21019 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr3:135996350-135997340 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF740 | MA0753.2 | chr3:135996446-135996459 | GTTGGGGGGGCGG | - | 6.27 |
| | | 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 |
| GH03I136277 | chr3 | 135996476 | 135997168 |
| Enhancer Sequence | CAGGGTGGGT GGAGGGGTAC AGCCAGGTGG GGGCTGGGTC AGGTGGGTCT ACACTCTGTC 60
TCTCCATGTG TGGGGAAAGC CGTGGCTCCT ATGAGGGTTG GGGGGGCGGT TCTCAGGTCA 120
TTAGGGTAAT GTTCCAGAGA GGAATATAAC TGCCTCTACT GCACAGAAGA GATCGCACAG 180
TGTGTGGGGA GTAACAGGTG GCACTAAGCC TCACCCAGAT CCCACACGGT CGGAAAGGCA 240
GATCTCACTC CCTCTGTGCT CTGCTAGCTG CACTGGGCTA AGTTCCAGGC AGCCTAGGCT 300
CAGAACTCAA ACCTGCCCCA GGCCATAAGC TTTCCCTGTG GGAAAGCAGC TGTGGCTTTC 360
AGGCCATGCT CCTCCCAGGC CACCTGCAGG GCCAGGCACC TGGCTCCTGC ACTTGTGGCT 420
GCAGTGCACT TCCCCCTGCC CCTGGGAGGT ATGGGTTCTG GACAAAGGAG TTCATCCTCA 480
CTCAGTGTTA TATCTTGAAA TGGGGAGATT CTTTCAACCT GCGACCACTA CCTGAGCTTG 540
TTGGCTGACT TCCCCAAGGT CCCCTGTGAG GTACAATAAA GAATGGCTTA CCTTGGTCTG 600
CACTGGAGAC TGGGAATGCC TGCAAAGCAC TTCCCGCCAC TGTTTCTACT TTTATATTTC 660
TTACTGCTCC CTAAATCAGT CCCAGCCCTG GGTAAGGTTA AGGCCTTCCC CCATGGCCTG 720
GATTTTCAGG TTCCCCAGTG GGAACCTGAA AGCAGCTTCT CTCTATCTCA CACTCTGGAG 780
ACTTACAGTT TTTCCCTTGT CTTATGGTTT AGGCTGCAGA CTGCCACTTC TTTAAAAGGT 840
CTGTGGATTC TTTCAGTTTT CCTGTTAAGT TCCTGCGTGG CTTCTTGGAA AAAGAGTCAC 900
CATGTGATTC TCAATACACT ATTCTGTTCT TCTAAGTGGG AGAGGCATGC TAACACTGCT 960
TCTTATCTGC CATCTTGGTG GGGGTGGAAA 990
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