Tag | Content |
---|
EnhancerAtlas ID | HS048-02975 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:192669480-192670400 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr1:192670285-192670300 | AATTAATGATTAACT | - | 6.36 | HNF1A | MA0046.2 | chr1:192670285-192670300 | AATTAATGATTAACT | + | 8.73 | HNF1B | MA0153.2 | chr1:192670286-192670299 | ATTAATGATTAAC | + | 6.05 | HNF1B | MA0153.2 | chr1:192670286-192670299 | ATTAATGATTAAC | - | 7.22 |
|
| 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 |
GH01I192699 | chr1 | 192668846 | 192672409 |
|
Enhancer Sequence | ATTAAACAAA TAGGTCATAT GCATAGCATT CATGATAAGT ATTTGGTAGA TAAAAATGAG 60 GATCTGAATA AACTTCCATG TCCTTCTCAC AGTGGAACTG GTAAAACACT TTAGCTGGTA 120 AAACAGTAAC TGGTAAAACA CTTAGCCATA CTAATGGCTA ATAAAATAGT CTGTTCTGGT 180 GTGAATTTCT CTTTTATTTA GCATCTTGTT TTTCTTTAGT GGGTAATTCA CTGGTTTTGT 240 GCAATCCTAA TCTACTATGA ACATTGATTT CTTGAGTATC CAGATATTAT TTTCAGAATC 300 TAGTTTTTCA CATGCTGAAA GTTCAAGTTT GAGATCCATC ACTACATGGC AATAATATTT 360 ACTCATGATG AAAATATTTG CCAGTCACTA TGTTAAATAT CTTGCATTTA CTGTCTTATA 420 TCCTATTTAC AAAACCTTGC AAGGTAGATA TTTTTACTTC CTTTTGTAGT TGAAAAAACT 480 CAAGCTTATG GGGATTTTGT AAATTCTAAA CTCACACAGT TGGGAAATGG TGAACTGTAA 540 TTCAGATGCA GACTGTCTAA TTCTAAGCTG CATACTCACC CACCTTACAG CTGAGGAGGG 600 AATGTTGTTC TAATAACAAG CCTTGCAAAA TGTCAGCTGC ATGCTTTACA TGCTAACCAA 660 GATTACATTC TTCCTCTGTT TATGTGGTTT TCTGAGCTCT GGGTAAGGCA ACTATTCTCT 720 GTGCCACAAA AAAAGTGTTT TATTCAGTTT TTTCTGGAGG AAATAAGGCT AATGCTGTTT 780 TCTATGGAGA AAAGCATAAT TTCCAAATTA ATGATTAACT TGAAAATGGA TGATTCATTG 840 GGCAAGCATT TCCTATACCA CAGCATTACA TGTTTTCCAA TTATAGTGCT CAGGGGAGGT 900 TCTTAGTTAA TTCTTAGTTC 920
|