| Tag | Content |
|---|
EnhancerAtlas ID | HS091-25338 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr2:24318100-24319180 |
Target genes | | Number: 13 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFKB1 | MA0105.4 | chr2:24318204-24318217 | AGGGGATTTCCCT | + | 6.15 | | NFKB1 | MA0105.4 | chr2:24318204-24318217 | AGGGGATTTCCCT | - | 6.1 | | REL | MA0101.1 | chr2:24318205-24318215 | GGGGATTTCC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TAACTGATTC ATCTCACTGG GACTGGTTTG ACAGTGGGTG CAGCCCACGG ATGGGGAGCT 60
GAAGCAGGGC AGGGCGTCAC CTCACCCTGG AAGTGCAAGG GGTCAGGGGA TTTCCCTTTC 120
CTAGCCAAGG GAAGCCGTGA CAGACTACCT GGAAAAATGG GACACTCCTG CCCAAATACT 180
GCACTTTTCC CAAGATCTTA GCCACCGGCA GACAAGGAGA TTCTCTCCCA TGCCTGGCTC 240
GGCGGGTTCC ACACCCACGG AGCCTTGCTC ACTGCTAGTG CAGCAGTCTG AGATCGAACT 300
GTGAGGCGGC AGCCTGGCTG GGGGAGGGGC GTCCGCTGTT GCTGAGGCTT GAGTAGGTAA 360
ACAAAGCAGC CGGGAAGTTC GAACTGGGCA GAGCCCACTG CAGCTCAGTA AGGCCTACTG 420
CCTCTAGACT CCATCTCTGT GGCCAGGGCA TAGCTGAACA AAAGGCAGCA GACAACTTTT 480
GCAGACTTAA AGGTCCCTGT CTGACAGCTC TGAAGAGAGC ATTGGTTCTC TCAGCACGGT 540
GTTTGAGCTC TGAGAACGGA CAGACTGCCT CCTTAAGTGG GTCCCTCACC CCCATGTAGC 600
CTAACTAGGA GATACCTCCC AGGAGGGGCC GACAGACACC TCATATAGGC ACCTGCCTCT 660
CTGGGACGAA GCTTCCAGAG GAAGGATCAG GAAGTAGTAT TTGCTGTTCT GCAATATTTG 720
CTGTTCTGCA GCCTCCGCTG GTGATACCCA GGAAAACAGG GTCTGGGGTG GACCTCCAGC 780
AAACTCCAAC CGACCTGCAG CTGAGGGACC TGACAGTTAG AAGGAAAACT GAAAAACAGA 840
AAGGAATAGC ATCAACATCA CCAAAAAGGT CATCTACACC AAAACCCCAT CTGTAGGTCA 900
CCAACATCAA AGACCAAAGG TAGATAAAAC CACAAAGATG GGGAGAAACC AGAGCAGAAA 960
AGCTGAAAAT TCTAAAAATC AGAGTGCCTC TTCTCCTCCA AAGGATCGCA ACTCCTCGCC 1020
AGCAAAGAGA CAAAGCTGGA TGGAGAATGA CTTTGACAAG TCGACAGAAG TAGGCTTCAG 1080
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