| Tag | Content |
|---|
EnhancerAtlas ID | HS098-10254 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:64333760-64335070 |
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 | TTATCTTGAA ATAAAACTGA AGTTTAGGAA AACGTTTCTT TTATGCTATA TTTAACCACA 60
TATGGGTTAT GATGGCAAAT ACTTGCTACA TCTTAGAACA AAGATAGATC AAATGCCTTT 120
TTTAAAAAAC TTCAATTTTT TTCTGATAAA TCAGAAGGAG TGCTCTCACT GCAAACACCC 180
GGGACCAGTT TTTTTTTTTA AAAAAAAAAA AAACCTTCCA GGATTCCTCA GTTCTCCCAG 240
GGGCCGGCTC TGCAACCTTT GTTATTCAAA TCAGAGGCTT TGAAGCTGGT GACCTTGTGG 300
GTTTTCCTGT CTTGTTAACC CAGTTGTTAT CTGTCCAAGG CTCCAGTGTC GGCCGCTTTG 360
AGCACCAGCC CAGTGACTCT CACGTCACTC ACATAAACTT CATGAAACAC CGCGGCTTGT 420
GCGATTTTAC TCTGATGTTG TTGGGCTGGT GTTGTCCGAT GTTTATTGGG TGATGCAATC 480
AGGTGACGCC TAAGGGGAGG GCTGGGAGGA GCATCTGGGT TAAGCAGGGA GAGCACAGAT 540
TTTAAACGTG GCCGAGAAGA ATTTTACCTT GCAGCCAGTT GTGGATCCAA ATCCCATCTC 600
CAAACCATGA GAATTTAAAT ACCGTAAATT CAGCTACTCG TGAGCCAGTG GGGTGGGGGA 660
GTGGGCAGAA AGCAGACCCT GAGATGGAGA AGGGAAGGCA AGGGGAGATG CAGCCACAGC 720
CTGGGCCCAG CCCAGCCCCT GGGAGCGTGG GAGCTGGGGC CTTTCTGGGT GGTCCCTCTG 780
CCCCATGAAC CAGTCACAGG CTGCTCTCCC CAGAGAAGGG GCAGCACTCC CAGGGGCTGG 840
GGGACAGGCT CTCCATCCTG AATGTGGTCT GGGCAATGCA GCCCAGGGTC TCCCGAGAGG 900
CCCTGTCCTG CCATGATTCC CATCTTCCAA GAGAAAGGCA CAGTGTGACT GGTTATCAGA 960
ATCAAAGCCA GAGAGGGCTA GTCCGGAAGT GAGGGGCAGC TCAGAGGCCC CCGAGGGCAG 1020
ACTTGGTCCC AGCCAGAGAG GCAACGCCCC AGCGCATCGC TGCCCCTGAC ACAAAGCCTG 1080
TGTGTGAAGG GATGGTGGAG CCACCCTGCC TGCCCTTTCC TGGAAGAGCC TGACGCTGGG 1140
GTTGTGTCCT GAGTTTGGCA GGCTTCTGGG ATCGCTGGCC GAGACAAGCC CAGGATTGTC 1200
CTCCGGGGTT GGCCATGTCC TCCCAGGCAG CTCCTGGTGG GAGGTGCTGT TGCTGTTGGG 1260
GTGCCCTCTC CCCGGCAGGG CAGGGACCTG ACTTCCAGCC TTGCCCGCAG 1310
|
