| Tag | Content |
|---|
EnhancerAtlas ID | HS048-14144 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr16:28543370-28544570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFKB1 | MA0105.4 | chr16:28543618-28543631 | AGGGGGATCCCCC | + | 6.02 | | NFKB1 | MA0105.4 | chr16:28543618-28543631 | AGGGGGATCCCCC | - | 6.03 | | NFYA | MA0060.3 | chr16:28543830-28543841 | GGCCAATCAGA | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 28543579 | 28543953 | | chr16 | 28543389 | 28544200 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I028531 | chr16 | 28543123 | 28546830 |
|
Enhancer Sequence | GTCTCAAAAA GGAGAAAACT GAGGGTGATT CTGAAATTTA AAAATGTACT CCTGTATCTG 60
TGAGCTGGCC TTTGAGAAAG GGGAAGGTGG AAGAGAATCA GGTTGCTTGC AGAACAGACA 120
GACAACCCCA TGGTGAGTTT CTCAGTTCTC TGCAAGGAGT CGGGAGTCCT TTGAGTTACA 180
GAAGCCTGAC AGGGCCAATT CTGTAAGCCC CTGGGGTAGG ACAGAGGTCA GTGATTTCTC 240
TAGTTCTCAG GGGGATCCCC CCAAAATGGG GAAACAGACA TGCAACCAGA AGAAAAAGAA 300
AGGGTTTAGG AAAGGGGATG GAGACAGAAG AGGAAGAGTC TGGGTAGGAT CCTTTCGGAT 360
CCAAAAATTC TGCAATTCCA AGAATTGCCT TAATTCCCAG AACAGCCACT TAAAGGCCTC 420
TCAGGCAGAG GCTGTGCCAG GCGAGGGCGA GGCCAGGAAA GGCCAATCAG AGGCCAGGAG 480
GGAGGGGCAG TGTGTGAGGA CTCCTGGCTG GTGTCAAAGG ACCCAGGACA GGGAGTGGCC 540
ATTCCAGCTA GGGACACAGT GCTTCCCAGC CTTCATTTTC TCTTTTGACA GAAGAGAGGC 600
CAGTCTCACC ATTTGACAGG TGAGGAAACC CAGGCCCAGA GGAGTAATTG ACCAGAAATT 660
AACGAGAGTT TAGGATTCTT CATTGTCAAT ACATGGTTCT TCCCAGGCAT GTAGCAAAGG 720
GGGAAAAATC CAGGCTTTAA AATTCAGATA GACCTGAGTT CATAATTCCA AGTCCTACAG 780
GATGTGGCTG TGTGACTTTA GGCAAATTAC TTAATGTCTC CGAACCTCAG TTTTCCGGTC 840
TGAAAAAAAG GGGATCATTA ATAGTATGTC CTATTGGGTT ATCGTAAGGA TTAAATGGAG 900
CAAAGCCTAT AAAACACTTC TCACAGAATA GGAGCTCCAA ACACAGCAGA GATGTTTCCA 960
GGATTTTCTG AAGCCAACAC ACCAGGTCTG TGCTGGGCTG AGGGCCGACT GCCTGGTGTT 1020
GCTCCTGCCA TTTGCTCCCT GGGTTCTAGA GCTGATGGTG GCCCTATTCC TGGTTCCAGT 1080
CATATCAGGA TTCTATTTGT CCCTCTCAGC AGCACAGGCC TCCAGCAGCA TCCTGGTAAC 1140
TCAGAAGGCA TCCAATAAGC ATTGATTGAG TTAATATGTA ACTTGTATGG AAAGAGGAGT 1200
|
