| Tag | Content |
|---|
EnhancerAtlas ID | HS048-03859 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr1:245560750-245562020 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr1:245561537-245561548 | AAGCAATAAAA | + | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGGTGATCC ACCCTCCTCC GCCTCCCAAA GTGCTGGGAT TACAGGCATG ATCCACTGCG 60
CCTGGCCCAC ATGTTCATTT CTAGCTTGTT AACTTTATTG TATTTACCAT ACTCTCCCAC 120
TTTTTAAACT ACAGATTCCT TGTAGAAAAA TGAATAAATG AATGAATGAG TGAAGGAAAG 180
TCAGTGGCAA TAACTAATGA TGTTTTTAAA ATTGTGTAGT AAGTGGCATA GTTATGAGAT 240
TTGGGGGATT TGGGGCTGGA TCAGACAGAG AAAACAGAAG GGGAACATGC CAGTGTCTTC 300
AAATGTTTGA GACACTGTAG TTTGGAAGAG ACAGCGGACA TGATTTTTAT TGCTCCTGAG 360
AATAGAATAG GAGCCAATGA ATAGACTATC CATTAATTGA TTTGTTCATT TCTAAGTTAT 420
TTCTTATGCA CCTGCTCTCT AGGGCATGTG GACGAGGTCC AGATGAGGAC AAGTTTCCTG 480
CTCTCAAATT TCTTGCATTT TAGGGAAGTA ATTTTTGGCT GACTTGCAAA GAACTTTCTA 540
ATGAGAAGAG TTATATAACC ATGGGATGTG TTGCCTTGTG AAGTAGGGAG CTTTCCATCT 600
TTGGAGAATC TCAAAAAGGG CTGAATGAAT ACCCTGAAAA ATACTACTCC CTCGGGAGAG 660
AAGGTGGATT TGTTGACCTC TAGGGTTTGG CTCTACTGTG CTTCCATGTT TCTCTTTTAT 720
TTGTCAGTTT CCATCTTAAA CTGAAGGATT AGGTCATTTC AGGGAGTTCT GGAGGTGAGG 780
TGGTGGGAAG CAATAAAAAT ACCTTCACAA ACCAGTTCCT TTACTCTTTG ATCCAGGTGG 840
TTCCCACAGG TCCCTTGACC CCCGATAAAG TAATCCCGGC TGCCTGCGAC GGAGGTGTAG 900
GCAGCCAGGG TTCATGGAGC CTGTGGTTAT CTCCTTACAG AGAGCCTTAT CAGCTTGTGG 960
AGCCACCGTA AAGCTTGCTT TGACCTTTGG CAGAGACTCC TCCTGTATGT CTGTCCACAG 1020
AAATGAGAGC AGGTGACAGA CACCTGGGAT GATCCTGAGA CCCAGCACCC AAAGCCCAGG 1080
CTTCTTTCTA TGGGGAAGTC AAGCAGAGGG ACCCAAGCTC ATAGCCAGTG GAGGGGTGGG 1140
TTGATGAGAG GCGAGCCCTT TACCAGATGT GAGCCCAGTC ATCACTCTGC ATTTTCTACG 1200
CAAAAGTCCA GGGGCTTGCT ATTGAAATTA GGCAAAGAGG ACAAAGAATT GCCCTCTGTA 1260
AAGTCCTCAA 1270
|
| |
|
|
|
