| Tag | Content |
|---|
EnhancerAtlas ID | HS180-04701 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:226221850-226223060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr1:226222154-226222165 | TGATTAGATTA | - | 6.32 | | IRF1 | MA0050.2 | chr1:226221935-226221956 | TTTTTCTTTCTTTTTTTTTTT | + | 6.59 | | KLF4 | MA0039.3 | chr1:226222483-226222494 | ACAGGGTGTGG | - | 6.14 | | SOX10 | MA0442.2 | chr1:226222870-226222881 | TTCTTTGTTTT | - | 6.62 |
|
| | 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 |
| GH01I226033 | chr1 | 226220902 | 226224392 |
|
Enhancer Sequence | AGTAACTCAC ACCTTTGTAT AATCATATAA TTCCCTCCCT TTGAGTGTGG GTGGGTCCAG 60
TGACTGCTTC TTTTTTTTTC TTGTTTTTTT CTTTCTTTTT TTTTTTTTTT TTTTTTTTTT 120
TTTTTTAAAG AGATGGGGTC TCACTGTGTT GCCTTGGCTA GAGTGCAGTT GCTGTTCACA 180
GATGCAATTA TAGCCCACTA CAGCCTCTAA CTCCTGGGCT CAAGCAATCC TTTTGCCTCA 240
GCCTCCCAAT CTAAGACTAC TTCTAACCAA CAGAATATGG CAAAGGTGAT GGGCTGTTAG 300
TCTGTGATTA GATTACATTA TATACAATTC TACCCCACTA GCTCTGTTCC TCCCTTAGTG 360
GCTTTGAGGA AGCAAGCTGC TATTTTGTAA GAGGACCTAT CAAGAGGTCC ACATGGCCAG 420
GAACTGTGAG CAGCCTCATA GAGCTAAGGG CAGCTAACAG TCAGCAAAAA TCCAGGCCCT 480
TGGTCTTACA GCAGCAAGGA ACCAAATTCT GCCAACAACC CGAATGAGTT TGGCAGCAGA 540
TCTGTCACTA GTCAGGCCTC CAGATGGAGC TGAGCCACGG CCGACACCAT GATGACAGCC 600
TTGCGGCCTG CACTATGCCC AGGCCCCTGA CTCACAGGGT GTGGGATAAT AAAGGGAAGT 660
TGTTTTAAAC TAGTGCATTT GTCGTAATAC GTTATGCAGC ATAGGAAACA AATATGCTCC 720
CTTATCCTAT AAGCCTCCAA TCTGAGCAAG ATGGCCTCAG CCCTTCTGCT TTTTCTTCTG 780
ATAACCTTTA CTCCATGTCC GCTAATGAGC AATTCTTTTT TATCTTATTT TATTTTATTT 840
ATTTTATTTT TTTAAGACAG GGTCTCTGTC TGTTGCCCAG GCTGGAGTGC ACTGGCATGA 900
TCATAGCTCA CTGCAGCCTC GACCCTGGCT CAAGTGATCG TCCAACCACA GCTTCCCGAG 960
TAGCTGGCAC CACAGGTGTG TGCCACCACA CCCGGATTTT TATAGGTTTT TTTCTTTTCT 1020
TTCTTTGTTT TTTTTTTTGT AGATGCGGGG TCTCACTATG TTCCCCAGGC TGGTTATGAA 1080
CTCCTGGCCT CAAACGATCC ACCTCGGCCT CCCGAAGTGT TGGGATTACA GGTGTGAACC 1140
ACCACGCCCG GCAGCAATTC TTAGGGTTTA AATAAACGTA TTGCTTTTTT CTCTTATTAG 1200
GAAAGTAAGA 1210
|
