| Tag | Content |
|---|
EnhancerAtlas ID | HS145-04415 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr11:64333590-64334630 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:64334445-64334466 | GGAGAAGGGAAGGCAAGGGGA | + | 6.34 |
|
| | 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 |
| GH11I064564 | chr11 | 64332189 | 64335552 |
|
Enhancer Sequence | CTCTCATCGC TACTAAAAAT CAAAAAATGA GGCAGGAGGA TCACTGGAGC CCAGGAGATA 60
GAGGCTGCAC TGAGCTGAGA TTGTGCTACT GCACTCCAGC CTGGGCGACA GGGCAAGATT 120
CCGTCAAAGG AAAAAAAAAA AAACCTAAGG ACCTGGTTTG ATTGGGACTT TTATCTTGAA 180
ATAAAACTGA AGTTTAGGAA AACGTTTCTT TTATGCTATA TTTAACCACA TATGGGTTAT 240
GATGGCAAAT ACTTGCTACA TCTTAGAACA AAGATAGATC AAATGCCTTT TTTAAAAAAC 300
TTCAATTTTT TTCTGATAAA TCAGAAGGAG TGCTCTCACT GCAAACACCC GGGACCAGTT 360
TTTTTTTTTA AAAAAAAAAA AAACCTTCCA GGATTCCTCA GTTCTCCCAG GGGCCGGCTC 420
TGCAACCTTT GTTATTCAAA TCAGAGGCTT TGAAGCTGGT GACCTTGTGG GTTTTCCTGT 480
CTTGTTAACC CAGTTGTTAT CTGTCCAAGG CTCCAGTGTC GGCCGCTTTG AGCACCAGCC 540
CAGTGACTCT CACGTCACTC ACATAAACTT CATGAAACAC CGCGGCTTGT GCGATTTTAC 600
TCTGATGTTG TTGGGCTGGT GTTGTCCGAT GTTTATTGGG TGATGCAATC AGGTGACGCC 660
TAAGGGGAGG GCTGGGAGGA GCATCTGGGT TAAGCAGGGA GAGCACAGAT TTTAAACGTG 720
GCCGAGAAGA ATTTTACCTT GCAGCCAGTT GTGGATCCAA ATCCCATCTC CAAACCATGA 780
GAATTTAAAT ACCGTAAATT CAGCTACTCG TGAGCCAGTG GGGTGGGGGA GTGGGCAGAA 840
AGCAGACCCT GAGATGGAGA AGGGAAGGCA AGGGGAGATG CAGCCACAGC CTGGGCCCAG 900
CCCAGCCCCT GGGAGCGTGG GAGCTGGGGC CTTTCTGGGT GGTCCCTCTG CCCCATGAAC 960
CAGTCACAGG CTGCTCTCCC CAGAGAAGGG GCAGCACTCC CAGGGGCTGG GGGACAGGCT 1020
CTCCATCCTG AATGTGGTCT 1040
|
