Tag | Content |
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EnhancerAtlas ID | HS184-19171 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr22:19767220-19768290 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GSC | MA0648.1 | chr22:19767359-19767369 | GGGGATTAGC | - | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 2 | ID | Chromosome | Start | End |
GH22I019779 | chr22 | 19767227 | 19767350 | GH22I019780 | chr22 | 19767440 | 19768630 |
| Enhancer Sequence | CCAAAAATGC CTTAAACACC TCAGTACAGA CACCCACACA CTATGAGGAT GATTCCCTCA 60 AACTGGTTCT GAAAGCAGTA GCTGTGCTTT TCTCTATCGC GTTCTTATTC TTTCTCCGAC 120 GTGCTCTTAG CACCCTCCTG GGGATTAGCA TCCGACCCAC ATCACTCGGG AAAAGCCCTG 180 GCTGGCGGCT CCCAGGCGGA GGCACCACGG TGAGGCCAAG TGCTGCTGTC CAGTAAGCCT 240 GACTGCCCCC TCAGGCTCTT TCCCTTCACA TTTACTTATT TATTTTTTAA ATCGACATAT 300 AAAATTGACG TATTTATTGT GTAAACTTCT TACCACAAAA ATGAGAACTA TGTCAGGTGA 360 TGTATTTGCT AGTTAGCTAG ACTTAAGCAG GCCTTTAGTT TTCAGTTTTT AACATTGAGG 420 GAAAATACAC GTAAATCAAA TTTACCATCG TAGCCCTTTG TAAGTGTACA TTTCAGTGGC 480 ATGAAGTCCA TCCACATGAC TGTGCAGCCA TCACCACCAG CCATCTCAGA ACTCTTCATC 540 TCAGAAAACT GAAACTCTGT CCCCATTAAA CAAGAACTCC TCATTCCCCT CCCCTGGCAG 600 CCAGCATTCT ACTCTCTGTC TCTGTGAATC TGACTACTCT AGGCGCCTCA TGTAAGTGGA 660 ATCACACAGC ATTTGTCTTT TTGTGGCTGG CTTAGTTCAC TGAGTGTAAG GACCTCAAGG 720 TTCATCCGTG TTCTAGCCTG TGTCGGAACT CCCTGCCTTT ATAAGGCTGA ACACTATTCT 780 GTTGTATGTC TGTACCACGT TTTGTTGATT CATTCTTCTG TCAATGGACA CTTGGGTTGC 840 TCCCACCTGT TGGCTGCTGT GAGTAATGCC GCTATGAACG TGGGTATAGA AATATCTTTG 900 CAGCCCTGCT TTCAGTTCTC TTGGGTATTC TGCCACAAGA GGAACTGCTG GCTCATATGG 960 TAATTCTATG TCCAGGATTT TGAGAAATGA CCACACTGTT TTCCATAGCT GCTACTCCAT 1020 TTTTACATTC CCACCAATAG CGCACAAGGG TTCAGATTTC TCCACACACT 1070
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