| Tag | Content |
|---|
EnhancerAtlas ID | HS184-05712 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:64333840-64335070 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat4 | MA0518.1 | chr11:64334872-64334886 | CCCTTTCCTGGAAG | - | 7.25 | | ZNF263 | MA0528.1 | chr11:64334445-64334466 | GGAGAAGGGAAGGCAAGGGGA | + | 6.34 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 64334024 | 64334364 | | chr11 | 64334600 | 64335062 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I064564 | chr11 | 64332189 | 64335552 |
|
Enhancer Sequence | ACTTGCTACA TCTTAGAACA AAGATAGATC AAATGCCTTT TTTAAAAAAC TTCAATTTTT 60
TTCTGATAAA TCAGAAGGAG TGCTCTCACT GCAAACACCC GGGACCAGTT TTTTTTTTTA 120
AAAAAAAAAA AAACCTTCCA GGATTCCTCA GTTCTCCCAG GGGCCGGCTC TGCAACCTTT 180
GTTATTCAAA TCAGAGGCTT TGAAGCTGGT GACCTTGTGG GTTTTCCTGT CTTGTTAACC 240
CAGTTGTTAT CTGTCCAAGG CTCCAGTGTC GGCCGCTTTG AGCACCAGCC CAGTGACTCT 300
CACGTCACTC ACATAAACTT CATGAAACAC CGCGGCTTGT GCGATTTTAC TCTGATGTTG 360
TTGGGCTGGT GTTGTCCGAT GTTTATTGGG TGATGCAATC AGGTGACGCC TAAGGGGAGG 420
GCTGGGAGGA GCATCTGGGT TAAGCAGGGA GAGCACAGAT TTTAAACGTG GCCGAGAAGA 480
ATTTTACCTT GCAGCCAGTT GTGGATCCAA ATCCCATCTC CAAACCATGA GAATTTAAAT 540
ACCGTAAATT CAGCTACTCG TGAGCCAGTG GGGTGGGGGA GTGGGCAGAA AGCAGACCCT 600
GAGATGGAGA AGGGAAGGCA AGGGGAGATG CAGCCACAGC CTGGGCCCAG CCCAGCCCCT 660
GGGAGCGTGG GAGCTGGGGC CTTTCTGGGT GGTCCCTCTG CCCCATGAAC CAGTCACAGG 720
CTGCTCTCCC CAGAGAAGGG GCAGCACTCC CAGGGGCTGG GGGACAGGCT CTCCATCCTG 780
AATGTGGTCT GGGCAATGCA GCCCAGGGTC TCCCGAGAGG CCCTGTCCTG CCATGATTCC 840
CATCTTCCAA GAGAAAGGCA CAGTGTGACT GGTTATCAGA ATCAAAGCCA GAGAGGGCTA 900
GTCCGGAAGT GAGGGGCAGC TCAGAGGCCC CCGAGGGCAG ACTTGGTCCC AGCCAGAGAG 960
GCAACGCCCC AGCGCATCGC TGCCCCTGAC ACAAAGCCTG TGTGTGAAGG GATGGTGGAG 1020
CCACCCTGCC TGCCCTTTCC TGGAAGAGCC TGACGCTGGG GTTGTGTCCT GAGTTTGGCA 1080
GGCTTCTGGG ATCGCTGGCC GAGACAAGCC CAGGATTGTC CTCCGGGGTT GGCCATGTCC 1140
TCCCAGGCAG CTCCTGGTGG GAGGTGCTGT TGCTGTTGGG GTGCCCTCTC CCCGGCAGGG 1200
CAGGGACCTG ACTTCCAGCC TTGCCCGCAG 1230
|
