| Tag | Content |
|---|
EnhancerAtlas ID | HS105-14439 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:64333810-64335070 |
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 | TTTAACCACA TATGGGTTAT GATGGCAAAT ACTTGCTACA TCTTAGAACA AAGATAGATC 60
AAATGCCTTT TTTAAAAAAC TTCAATTTTT TTCTGATAAA TCAGAAGGAG TGCTCTCACT 120
GCAAACACCC GGGACCAGTT TTTTTTTTTA AAAAAAAAAA AAACCTTCCA GGATTCCTCA 180
GTTCTCCCAG GGGCCGGCTC TGCAACCTTT GTTATTCAAA TCAGAGGCTT TGAAGCTGGT 240
GACCTTGTGG GTTTTCCTGT CTTGTTAACC CAGTTGTTAT CTGTCCAAGG CTCCAGTGTC 300
GGCCGCTTTG AGCACCAGCC CAGTGACTCT CACGTCACTC ACATAAACTT CATGAAACAC 360
CGCGGCTTGT GCGATTTTAC TCTGATGTTG TTGGGCTGGT GTTGTCCGAT GTTTATTGGG 420
TGATGCAATC AGGTGACGCC TAAGGGGAGG GCTGGGAGGA GCATCTGGGT TAAGCAGGGA 480
GAGCACAGAT TTTAAACGTG GCCGAGAAGA ATTTTACCTT GCAGCCAGTT GTGGATCCAA 540
ATCCCATCTC CAAACCATGA GAATTTAAAT ACCGTAAATT CAGCTACTCG TGAGCCAGTG 600
GGGTGGGGGA GTGGGCAGAA AGCAGACCCT GAGATGGAGA AGGGAAGGCA AGGGGAGATG 660
CAGCCACAGC CTGGGCCCAG CCCAGCCCCT GGGAGCGTGG GAGCTGGGGC CTTTCTGGGT 720
GGTCCCTCTG CCCCATGAAC CAGTCACAGG CTGCTCTCCC CAGAGAAGGG GCAGCACTCC 780
CAGGGGCTGG GGGACAGGCT CTCCATCCTG AATGTGGTCT GGGCAATGCA GCCCAGGGTC 840
TCCCGAGAGG CCCTGTCCTG CCATGATTCC CATCTTCCAA GAGAAAGGCA CAGTGTGACT 900
GGTTATCAGA ATCAAAGCCA GAGAGGGCTA GTCCGGAAGT GAGGGGCAGC TCAGAGGCCC 960
CCGAGGGCAG ACTTGGTCCC AGCCAGAGAG GCAACGCCCC AGCGCATCGC TGCCCCTGAC 1020
ACAAAGCCTG TGTGTGAAGG GATGGTGGAG CCACCCTGCC TGCCCTTTCC TGGAAGAGCC 1080
TGACGCTGGG GTTGTGTCCT GAGTTTGGCA GGCTTCTGGG ATCGCTGGCC GAGACAAGCC 1140
CAGGATTGTC CTCCGGGGTT GGCCATGTCC TCCCAGGCAG CTCCTGGTGG GAGGTGCTGT 1200
TGCTGTTGGG GTGCCCTCTC CCCGGCAGGG CAGGGACCTG ACTTCCAGCC TTGCCCGCAG 1260
|
