| Tag | Content |
|---|
EnhancerAtlas ID | HS148-05108 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr13:50209190-50210630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr13:50209972-50209993 | AGGTACTTTCAGTTTTCATCT | + | 6.08 | | NFYA | MA0060.3 | chr13:50209871-50209882 | GACCAATCAGA | + | 6.14 | | NFYA | MA0060.3 | chr13:50209962-50209973 | GACCAATCAGA | + | 6.14 | | NFYB | MA0502.1 | chr13:50209866-50209881 | AAAGTGACCAATCAG | + | 6.47 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 50209291 | 50209522 | | chr13 | 50209681 | 50209984 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I049634 | chr13 | 50209127 | 50210806 |
|
Enhancer Sequence | GTGTCTTTTG ACCCAGGTAG ACACTACTGA CACATTGGTC TGCGCAAACA GTTCACCACA 60
GCTGCCCTTT CATGCCATAG GCTCGATTTT TCCTGTTCTC TTGGCAATCC CTCTGGTTCA 120
GCCAGGACAG TAGCCTCCTC TCTGACACCA AGATGGACCA TGCTCTTCCC CAGCTCCAAA 180
TGTGTGCTCC TTGATGGAAT AGACACAGTG GACAAGAGGA CCCTCAGGTG GCTTTGAGTA 240
TTTGCCTCAA GCCCATCATC CCTGAAGGCA GATGTGCTTG ATCTTAACAG AGCCCAGGAA 300
GTCTCCCCTC AGATACAATT TTGGAAAAAG GACAATGAAA ACAAAAAGTC ATAACTGTCT 360
AGGTTCTTTG CATTTTGAAC AAAGAATTGG ACAAAAAGCA CAAACAAAGC AACAAAAGAA 420
AAGCACAGAT TTATTGAAAC AAAAGTACGC GACACAGAGT GGGAGGGGGC TCGAGCAAGC 480
AGCTCAAGAG CTTTGGTTAC AGAATTTTCT GGGGTTTAAA TACCCTCTAG AGGTTTTCCA 540
TTGGTTACTT GGTTTACACC CTATGTAAAT GAAATAGTGG CCCACGATCA GTCTGATTGA 600
TTGCAGAAAG CAACTAATCA GAGGCTGAAG TGAAGATACA AAGTTACACC CTATGCAAAT 660
GTCTGATTGA TTGCAGAAAG TGACCAATCA GAGGCTGAAG TGAACTTACA AAGTTATACT 720
CCTCTGCAAA TGAAGACTTG GCCTGTGACC AGCCTGACTG GTTGCAGGAG GGGACCAATC 780
AGAGGTACTT TCAGTTTTCA TCTGCAATGC AGGGGAAGTT GGGGGGTTGC AAAGGGAGTA 840
GCCTCTGATC CTTTTGTTAT TTGGGTGTGG AGAGGTGGGC TTTTCTTTTT GATTCAGTTC 900
TAGGAATTCG GCGCGAATCA GCCTTAGGTT CCCTGCCTCC AGACCCTACT CTCCTGCCTC 960
AATAGCCATG CCCAGTTAGT GTTAACTGTA ACTCCCTGCT GGTCTGCCTC CTGCTAGGAG 1020
GGACTGAACA TCAAATCACT CGCATCGAAT TACTCAGCAG GTGAGTTCTG GGGATGATAA 1080
CCACACAATT CTCTCTGCAC GAAAGATGGG TTTGAGAGCC TCAGAGTCTG GGGGAAGCTC 1140
TGCCAGCCAT CCACTTACTG GCTTACTGTT TGCCTGAAGT AAGCATGGGA ATCCCACAGG 1200
GTACAAGGTC CCGCATACCC TTCTGGGATT TCCGATGCCC TCTTTGCATG TGCTCTGGTC 1260
CATCAAGCTC CCATGCCAGA TGCAGTGCTT GTAGTTGCAG CAGTGACCAT AGCAGTGGCA 1320
ACAGTTCTAC AGGGTCACAG AACTTTAGGG AAGCCTCCTA ACACCCCTGC TCTTCGTTAG 1380
GCTGCAGCTG CTTTCCTGTC CATGATTTAA GCATCCTTAG ATCCCAGCTG TCCAGGAAGC 1440
|
