| Tag | Content |
|---|
EnhancerAtlas ID | HS184-17519 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:233488500-233489710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr2:233489384-233489395 | ATGTAAACAAA | + | 6.14 | | INSM1 | MA0155.1 | chr2:233489219-233489231 | TGCCAGGGGGCA | + | 6.62 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_05264 | chr2:233488148-233489824 | Brain_Cingulate_Gyrus | | SE_06506 | chr2:233488026-233490411 | Brain_Hippocampus_Middle | | SE_07434 | chr2:233488345-233490829 | Brain_Hippocampus_Middle_150 | | SE_08495 | chr2:233488452-233490260 | Brain_Inferior_Temporal_Lobe |
|
| | 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 |
| GH02I232624 | chr2 | 233489261 | 233489410 |
|
Enhancer Sequence | GCCTGCGTGA GTGAAGGGAG GACAAGTGGG CAGAGGGCTG AGCTCCTTCA GAGGAAAGCA 60
TTGCCTCCTG GCCCCCCAGG TGAGAGCTGT GTGCAGGCCT GTGCAGAGAA GGGGAAGAGA 120
GAGCAGAATC GCCCCAGGGG CCAGAACCAA GAGTTGACCG ACCAGATGTA GGGGCAGACA 180
GCTGGGAGGA TGGAGCTTCC TAGGGCGGTG CCAGCCCCTG AAGGGCATGG GTGGGGACAA 240
GATGGGGCCA GGTGGGTCAT CTTCTTATAG CCATGCCCAG GGCTGTGGGG GTGGGGTCTG 300
CTCTCCCTCC CTGCAGCCGT TTAGGACTCA TAGGTTTTTT GCTGCTCCTG TCGGGTGAGG 360
AATAAGACTG ATGTTTTCTT TATTTTGGAA TCCTTTGTTG TTCTCTTGAT TCTCTGAGCC 420
TGTGGGGAGC TGAGCCTACC CAGGGAACCC AGGTCTTTGC TAATCAGCCC CCTGGGGGTG 480
CTCCCTATCA AGTCCCTAAA GTCCCCCAGC CCCAGCTTGC CCCCCAGACC ACAGACATGG 540
ATGACAGGAG CCACAGGGGG CTTTGGGAAC CAGGCCTCAC CTGGGGGTTA GAGCCTGTGG 600
GTCTGGCTTG GCGCCTGGAG TCTAAGTTTA AAAGCTCCCC TATTCTTGAT GCCTGATTCT 660
CTGATTCTCT GCCAGGAATT TCTCCAGCAG CTGTGCCAAC ACAGGGGCTC CAGGGCCTAT 720
GCCAGGGGGC ACCCTTGTGT CTGGCTTGCT GGGATTCATT TACACAGTCT GTGCTAATAA 780
AAGAGATGGG GAGAACCGCA TTTAGCTAGT GCCTGGGGGC TATCCACTGG GCACTGGCAG 840
CCAAGCCGGG GAAAGTTGTG TGAATCACTT TAAGGGTTTC CCAAATGTAA ACAAAGGCTT 900
GAAACTTGCC CTTGAGGAGA CATCCCTGGA GGAAAGGTGA AGTCATTGAG GGCTATCTAG 960
AAACATCTAT AGGGAAAGAA TTAGAGGAAA GGACACAATT GCCAGAAGAT GCTGGCAAAA 1020
AAGGAGGAGC TCCACGCTTA CAGCCTCTGT TTTTCAGTTC TAGCCCTCAA TTCACTGTTA 1080
GACCCCCTCA CTTTCTGCTG GTCATGATTT AAATGTCACC GACTCCATGA TGCCCCTCCT 1140
GGTCATTTTA CCTAAAATTA CAACTTGCCC CACCACTCCC GACACACTTT TCTTAGATGC 1200
TTTTCTGACT 1210
|
