| Tag | Content |
|---|
EnhancerAtlas ID | HS145-21212 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr5:125701160-125701790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GRHL1 | MA0647.1 | chr5:125701415-125701427 | AAAACCGGTTTA | - | 6.44 | | GRHL1 | MA0647.1 | chr5:125701415-125701427 | AAAACCGGTTTA | + | 6.92 | | STAT1 | MA0137.3 | chr5:125701407-125701418 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr5:125701404-125701418 | TTTTTTCCTGGAAA | - | 6.02 | | TFCP2 | MA0145.3 | chr5:125701416-125701426 | AAACCGGTTT | + | 6.02 | | TFCP2 | MA0145.3 | chr5:125701416-125701426 | AAACCGGTTT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH05I126366 | chr5 | 125701301 | 125701450 | | GH05I126365 | chr5 | 125701641 | 125701790 |
|
Enhancer Sequence | TGCTTTTTAA AATCTGGTAA CTCTGAGGTC AAATGTGTAT GTTTTATCAA ACACCCAAAT 60
GTGAATGTTT AAATGTTTAC AGCGGTGTAA GGGAGTCAGC TCATGCTTGC TCAACTGTCA 120
GTTCATTACA GGCTCAATTC CCAAAGTCAC GTTCAGTGTA TCATGTCAGC AGCTTGAAAT 180
CAGCTGTGGT AGGAGTATTT ACGCTGTGGA AATTGGCCAG TGCTACAAAT CAGAGCTTTT 240
TTTTTTTTTT CCTGGAAAAC CGGTTTACCA ATGCATCACT GTTTAAATAA TAAACATATC 300
AATCAACAGA AAGTTCTGCA AACAAAATTT TTAAAATCAA CTATCTCAAA TCATTTTATA 360
AATTTAAGCA AATATAGTTA AAAGCACTAA AAAGACTTAC CCAAGCTGGT GGATAAACTA 420
GAATAGGAAC TTGGGTTTTC AAATTTCTTA CCTTTATATC TTAAAGCCCC AAATGCACAC 480
AAAAAAAGAA AGATTATCTA AAGTCCAATC TTGCCATGTC TACTTACATG TTTACTGAAG 540
CTGCAAGATC AACTTTCTAA TCTTCTGGGG GCAAACTCCC TCTAAAGTCA TGAGCTGTGG 600
CAGATAGTAA TAGTTCTCTG ACAAGGGGAT 630
|
