| Tag | Content |
|---|
EnhancerAtlas ID | HS048-28017 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr4:82271730-82273100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr4:82272989-82273008 | TGCTGCCCTCTAGTGGCTA | - | 7.9 | | EWSR1-FLI1 | MA0149.1 | chr4:82271926-82271944 | AGAAGTAAGAAAGGAAGG | + | 6.58 |
|
| | 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 |
| GH04I081351 | chr4 | 82272901 | 82273050 |
|
Enhancer Sequence | CTTGTTTACT GTCTGTTTTC TGCACTAGAA AATGTTTCCT TAGAGCAGAA CCCTGGTCTC 60
AATTTGCCAG TGTGTTCCCA GTATGTGGCA TCAAGTAAGT TCTCAATAAA TACCTGTTGG 120
AAAGGACGAA TAAAGAAAAA AATGCTTGTA AGCAGAAAAG AACGAAGAGT TTGATCATTT 180
TAGAAGCAAG ACTAAAAGAA GTAAGAAAGG AAGGAGCTAA GAAGAAGAGT CCAAAATAGT 240
AGAAAGAACA AAAACAGGAG CCAGGGGCTG TCCTTCTCCG CCAGACAGTC CTGCTCAACC 300
ACCCACTCTG TTATCTCTCC TGCCAATGCG GCAGAGCATT TTAAAGGTAA AAAGATGAGG 360
GACAGGGATC AGCCATTATT GCTCACTTCA GCCCACCTTT ATGCTGGGTT CCCAGCCTGC 420
TTATTCTCTG TGAGAAGGCT GGAGGATGCA GCCACCTGGC CAGCCACAGT GTCCTGCCTG 480
GAACATGTCA GGTTGTGTAA GACCCTGGGA GGACCAGCAT GTTAGCCACA GTGTTTGCAC 540
TGGCACCTCT TCCTCCTTCT GCCAGGGCCA CGTATTCCTG GCCTTTGTCT CCCACTCAGG 600
AACCTGAGAC TCAGGCTTAA AAGGCTATGG AAGGGCAACA TGTATTCCCA ACAATGAACT 660
GTGAAGTCAC CTTACCCATA GTCCTGGCCT GTATTTACTA AGGGCTAATA AGCTGAGTTC 720
TTCATATGCC TTACTCCACT TAAGCCTCAC CACCCCTCCA GGAGGTAGCG ACTGTGGTTA 780
TCCACATTTC TCAGATGAGC AAACTGAAGC TGAGAGAATT AAATAACCTG CTCAGTATCA 840
CAAAGCCGAG TAAATGCTAG AACTGGCATA TAAACCCAGG CCAGTCAGCT TCTAAATGCT 900
TTTAAGCGTC ATTACCTTCA AAAGAGTAAA ACTCTACTTT GACCTTTCTT CTTGTCTTTG 960
GTACCTTGCT CTCAGGTTAG CCGAGTACCT GATTCCCTTT TCTTCCATTA TTGGTGTGGG 1020
GGATAAATAT CTAAGTACTG TATATTCATC TAATTTTCTC TGCTTAGTCA CCATGATTTC 1080
TAAAGAAATG TAGCGATCTT TGCATATCTG TTTAACTTTT CCATGGGGGT CATTGTAAGG 1140
GTTATTTTTT AGTTGTCTGC TTTTTCAGGG CTCCCTCCCA CCTGCTGTAG CCCCAGAAAC 1200
CATTCACACA CCCTTTAAAG CAGAGAAGTG ACATCTACCT GCTTACACTT TCTGGGCCGT 1260
GCTGCCCTCT AGTGGCTAAA GTAAATGCGG CTTCAGCTCA AGCCTCGTTT ACATCTTAAG 1320
AGCCCAGAAG CTACATGTTC TTAAAAGGCT CCCCGATATC CACATTTAAG 1370
|
