| Tag | Content |
|---|
EnhancerAtlas ID | HS091-08387 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr11:77597020-77597930 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr11:77597184-77597201 | GAGGTCACAGTGAGCTG | + | 6.48 | | KLF16 | MA0741.1 | chr11:77597802-77597813 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr11:77597803-77597813 | GGGGCGGGGC | - | 6.02 | | SP2 | MA0516.2 | chr11:77597800-77597817 | GAGGGGGCGGGGCAGGG | - | 6 |
|
| | 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 |
| GH11I077886 | chr11 | 77597481 | 77597710 |
|
Enhancer Sequence | AGGATTGCTT GAAGACAGGA GTTTAAGACG AGACTGGGCA AAAAAGTAAG ACCCCCCAAT 60
CTCCACACAA AAAAAATTAA AATTAGCCAG GTGTAGTGGT GTGTATCTCT AGTTCCAGCT 120
ACTCAGGAGG CTGAGGCAGG AGGATCCCTT GGACACAGAA GTTTGAGGTC ACAGTGAGCT 180
GACCATGCCA CTGCACTCCA GCCCAGGCAA CAGACAGAGA CCTTGTCTCA AAAAAAAGAA 240
AAAAAAAATT CCCAGCATTC TCAGCAAAAC TGTCCTTGGT GAAAGGCCTT CACTCCTCTG 300
TGAAATGGTT GCTGGAAGCC TTCTTTCATT TGTCTACTCC AAAAGTGGAG CTTAGAAACC 360
TGTGGCCCAA GTAGGTCAGA GGAAGGAAAT GGCCAGTATG AATGATCATC AGGTAGAATA 420
CAGTAACCTA GATTAGGCTT ACAAGAGTTA ATAATCGCGA AGGCCCGCGG CGGGTGTTGA 480
TGCCATGTGA TTTCTGCCCA GTGCTCTGAA TGTCAAAGTG AAGAAATTCA ATGAAGCACG 540
GGTAAACGGC GGGAGTAACT ATGACTCTCT TAAGGTAGCC AAATGCCTTG TCATCTAATT 600
AGTGACGCAC ATGAATGGAT GAACGAGATT CCCACTGTCC CTACCTACTA TCCAGCGAAA 660
CCACAGCCAA GGGAATGGGC TTGGCGGAAT CAGCAGGGAA AGAAGACCCT GTTGAGCTTG 720
ACTCTAGTCT GGCAGGGTGA AGAGACACGA GAGGTGTAGA ATAGGTGGGA GGCGCCCGGC 780
GAGGGGGCGG GGCAGGGTCC GCAGGCCTTG CTAAGAAACT CACTCAAAAC CGCTCAACTA 840
CATGGAAACT GAACAACCTG CTCCTGAATG ACTACTGGGT ACATAACGAA ATGAAGGCAG 900
ACATAAAGAT 910
|
