| Tag | Content |
|---|
EnhancerAtlas ID | HS048-03535 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:226221890-226223050 |
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 | TTGAGTGTGG GTGGGTCCAG TGACTGCTTC TTTTTTTTTC TTGTTTTTTT CTTTCTTTTT 60
TTTTTTTTTT TTTTTTTTTT TTTTTTAAAG AGATGGGGTC TCACTGTGTT GCCTTGGCTA 120
GAGTGCAGTT GCTGTTCACA GATGCAATTA TAGCCCACTA CAGCCTCTAA CTCCTGGGCT 180
CAAGCAATCC TTTTGCCTCA GCCTCCCAAT CTAAGACTAC TTCTAACCAA CAGAATATGG 240
CAAAGGTGAT GGGCTGTTAG TCTGTGATTA GATTACATTA TATACAATTC TACCCCACTA 300
GCTCTGTTCC TCCCTTAGTG GCTTTGAGGA AGCAAGCTGC TATTTTGTAA GAGGACCTAT 360
CAAGAGGTCC ACATGGCCAG GAACTGTGAG CAGCCTCATA GAGCTAAGGG CAGCTAACAG 420
TCAGCAAAAA TCCAGGCCCT TGGTCTTACA GCAGCAAGGA ACCAAATTCT GCCAACAACC 480
CGAATGAGTT TGGCAGCAGA TCTGTCACTA GTCAGGCCTC CAGATGGAGC TGAGCCACGG 540
CCGACACCAT GATGACAGCC TTGCGGCCTG CACTATGCCC AGGCCCCTGA CTCACAGGGT 600
GTGGGATAAT AAAGGGAAGT TGTTTTAAAC TAGTGCATTT GTCGTAATAC GTTATGCAGC 660
ATAGGAAACA AATATGCTCC CTTATCCTAT AAGCCTCCAA TCTGAGCAAG ATGGCCTCAG 720
CCCTTCTGCT TTTTCTTCTG ATAACCTTTA CTCCATGTCC GCTAATGAGC AATTCTTTTT 780
TATCTTATTT TATTTTATTT ATTTTATTTT TTTAAGACAG GGTCTCTGTC TGTTGCCCAG 840
GCTGGAGTGC ACTGGCATGA TCATAGCTCA CTGCAGCCTC GACCCTGGCT CAAGTGATCG 900
TCCAACCACA GCTTCCCGAG TAGCTGGCAC CACAGGTGTG TGCCACCACA CCCGGATTTT 960
TATAGGTTTT TTTCTTTTCT TTCTTTGTTT TTTTTTTTGT AGATGCGGGG TCTCACTATG 1020
TTCCCCAGGC TGGTTATGAA CTCCTGGCCT CAAACGATCC ACCTCGGCCT CCCGAAGTGT 1080
TGGGATTACA GGTGTGAACC ACCACGCCCG GCAGCAATTC TTAGGGTTTA AATAAACGTA 1140
TTGCTTTTTT CTCTTATTAG 1160
|
