| Tag | Content |
|---|
EnhancerAtlas ID | HS180-10382 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr11:133097640-133098750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx3-2 | MA0122.3 | chr11:133098275-133098288 | ATAAACACTTAAC | + | 6.08 | | TCF3 | MA0522.2 | chr11:133098177-133098187 | AGCAGGTGTT | - | 6.02 |
|
| | 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 |
| GH11I133228 | chr11 | 133098421 | 133098570 |
|
Enhancer Sequence | CAGCAGCCAG GAGGCCACCT GCCTCCCCAG AGAGTGCCTT TTCATCGCCA GGAGCTGCAG 60
TTACAGTCTC CTAGGGGTCC CAGCAAAGAA GCATTCGACT TAATCGCTAA GATGCCCTGC 120
GGTGCAAACG CTGGGCCCTG TGACCACATG CAAAAGGAAG TTGGGTCAGG CTTTGGCCCA 180
GAGCGCGACA TGACCAGTGT CCATTTCCTG AGCAGCAGTG GAGTGCCCCG ACCAAGTCTG 240
GGAACCTGGG GACTCTGCCC TGAGAGCTGG GGCTGGGTTG ATCCAACTTC TTAGGTGAGG 300
TTTTCATCTT TATTGGGAGA CCTTTGTCCT TGGGATGGGA GATGTCCCAT TCATTAATTA 360
TTGTGCTGGC TCTGAATAAT TGCGGCCAGA GACTGCTATG CTGGGCAATT TCCAGTTCTA 420
CCGTGGCTGC TGCCGTGACA CTGTATACGT CTTTCACTGG TACCGCACTG CATTTTACAA 480
GACATGGTCC CTTCACCCGC TCAGCTGTTC CCCATAATAA CATGAGGAGG TGAGCATAGC 540
AGGTGTTCAC ACCCCGGTTT TACAGACAGA AACAGTTGGA AACCTGGAGG CCGAGGTTCA 600
TAAAGGTTAA ATGTGGTGAA GGTCACACAG CATACATAAA CACTTAACAA AACAGGACTA 660
GATTCCTAGT TTTCTGCTTC TAATTCCAGT TCTTTCCGCT ATAGCTCATG GAAACAGAAT 720
CTCAGAGAGA GTTTTCAAAC TCATCCACAG TCCCTTCAGC ACCTTCGCGG GCCAGCCACA 780
AGCCGAGGTG CCCGCTGGTG CTCAACAGCG CCAAAGCGTG TGGCCCCTCC CAGGACGCTG 840
CGCCCTGCCG GGCCTCCCCG TCCTAGAGCT CTGCTTCTTG CCACCTGCCC CCGCTTGGGC 900
TGCCCCTCCT ACTGCTCTCG CTGCCAGGCA GCTTGGGGCC TCCCACGAAT TTATGGAAGG 960
AGATTGGCTC CTGCAGAGCC CCTCAGCACG GGCCCAGGAG GCTTCGCATG AAAAATGATT 1020
GCACCGCACA CGCGGAGGCT GTTTAAACCT GTCACTTTAA AATATCCCTT CTCCTCTGCC 1080
CAAGCTGGGC CAAGAGGAGC AGGTCCAGGA 1110
|
