| Tag | Content |
|---|
EnhancerAtlas ID | HS147-10029 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr11:114286840-114287890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr11:114286959-114286970 | TCAAGGTCAAA | + | 6.14 |
|
| | 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 |
| GH11I114416 | chr11 | 114286825 | 114287806 |
|
Enhancer Sequence | TTAGGGTTGA GAACTCTAGT ATCATACTAT TTTTATTCCC ATGGTGCTTC CCCTTAAATT 60
CTCAGCAATC ACAAACTTGT CATTTTCTAT CAATGGACAG ACTGAAACAG TTGTATCAGT 120
CAAGGTCAAA ATCAGAGAAG CAGAACAAAG AGTGATCTAG AATAAGAGTC TGATTCTAGG 180
GATTCAAACA TTATGCCACT GGGATTGCTG GTGGAGTAAT CTGCTGGCCT GCATGTGGTG 240
CTGGGCCTGA AGTCACCGTG GGTCAGCCAG ACTAGCAGTT GGGAAGGAAA GGTGAACAAG 300
AACAAAAGCA GGAACCAACC ACAAACTTCT AGAAAAAGAT GGAGCTTACA TCTGTCTTTC 360
ATTACTCCAC CTTATGTGAC TTGGATGGCC TGAGGCCTGC AGGAGTAGCT GGCACCTCTA 420
GCTATAGGGC TGCACATATC TTTGGCCCAG AACACAGAGA AGTTTGAGGA GATGTGTCAG 480
CAGCTGGAGG AGCTGCTGGT TGGGTGCTGC CACATGCCAA CAAGGTGAGC CAACAAGGTG 540
AGCCAGGGGA TCAGCAACAA TGTGCATGAG GTTCCACAGT GCCTGGCATC CTGCATTAAT 600
CTTCCAGAGG GTAAAAATTA TGGCTGCTAC TTCCCTGTGA CTTCCAAATC TCAAGCAAAT 660
TTCTCTTGTG GTCAACTGCA TTGCAATTCT GACACTAACT GCTTGGAGTT AGGCCAAATT 720
TCACAGGCTA AGGGCTCAGT CCTCTATGAG ACTGCTCTCA ATTCAGACAT CAGCCACATG 780
CTCAGGGATT CCCAGGCCAC CCACACTTCT GGCCAACTGG CTACAAATTC AACAGTTTCC 840
ACTACTTTCT TAGGTTTAAT AACTTGCTAG AAAGACTCAC AGAACTTTGG AAAAAGCTAT 900
ACTTAAGATT ACAGATTTAT TAAAGCAAAA GAAAACACAT CAAAACCAGC CAAAAGGGGA 960
GATGCATAGA GTGAGACCCA GGCGGGTCCT GAAGGTGAAA CTTCTGTGTT CACTCCCTGT 1020
CACTGTGTAT TATCAGCCTG GAACCTTATC 1050
|
