| Tag | Content |
|---|
EnhancerAtlas ID | HS048-21080 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:113896090-113897480 |
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 | chr2:113896144-113896163 | TATCCACCAGGGGTCAGCA | + | 6.35 | | RREB1 | MA0073.1 | chr2:113896736-113896756 | TGTGTGTTGGTGGGTAGTGG | - | 6.12 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_26693 | chr2:113896004-113896910 | Esophagus |
|
| | 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 |
| GH02I113138 | chr2 | 113895561 | 113897437 |
|
Enhancer Sequence | GACGTCTTGC CTCTGGGTCT CCTTCATGTG GAGCTAAAAG AGTAGTTCAG GAAATATCCA 60
CCAGGGGTCA GCATTTTGTA CACACCTGAC TGCTCTGGAA AGTGTTTTTG TTTTTTTTTT 120
TTTAAATAGA AACGGGGTTT CACCATTTTG CCCAGGCTGG TGTCCAACTC CCAGACTCAA 180
GCAATCCGCC CGCCTCAGCC TCCCAAAGTT CTAGCATTAC CGTGTGAGCC ACCACACCCG 240
GCCTGGAAAG AATCTTGACA AGGCAAATAA TCAGTTTGGT TCATGCTCTC AAATTAGTGA 300
AGGTCTGGTT TTTCAAGACT CTCTAGGTGT TTCACTCTAA GGAAAAATTT ATTTTCATTC 360
ACCTATCAAT CAAGCTGAGG TGGGGCCTGA CTCCTGACAA GTATCCAAAT GTTGCCTATT 420
GCCAATGTCT AGTCTCCAAG GGGTGACACC CGAGAAATTC TAAGTCTTCT GTGCCTGCTT 480
TAAAGTCCAC TTCCTGTCAT CCTGTTATCT GTTGCAGACC TTTTACCTGT ATGATTGACT 540
GGTGTGTGGA ATTAACACTT CCCTCCTCGG CCGGGGGAAC ACACCCACAT GTTGGAACTC 600
AGCACAGGAA TCCCAACGGC GTGCCTACAA GGGAAATGCG TACTTTTGTG TGTTGGTGGG 660
TAGTGGACAG AACTCGTAAA AGAGATAGAT AAAATACCCA GGCACTCACT ACAGTGGGGA 720
ATGGATCTGT TCAGGGGCCA GCTATGCCTG CATTCTTTCC CAGGGACAGT TGACACAGTC 780
AGATGACTCA GGAAACTTGA TTTGCTTGGA GTCAGAGCAG AGGAAAGATC TTAGTGACCA 840
GGGACCTCAA GCTGCCCCAC CTGAGCGCTC CACCTCCACT CCAAGGGGCT TCCTGCCAAG 900
AGATCAGTAT GTCTGTGTGT AGAGTCAAGA CACATCTTCC TTAGGCCACA ATGGAGTCAC 960
ACTGACATCT TCGCCTTCCC TCCTTGGCAG TATTTATTAT AAGTCACAGG AGTTTAGTTT 1020
TCTTTCAACT CAGGCCTGTG GTTGGAGCAC AGGGAGCTAG GCTGGGGCTA GATCTTGCTA 1080
ACCTAGTAGG CAATGGTAAG GATTCTAGTC TGTCCTAAAG CATAAATAGG CCTTGGACAC 1140
TCTGAAATTT GTCCTTTCAC CACCCCATGC TCTACTTCTA AGTGCTCTCT CTCCCCATCT 1200
GCACCCCCTA GTTCCTACAA AAATCTCCTC AAAGCGAGGC TCTTGGACAA TTTGTTCCAT 1260
GAAGACATCG AGCACGGTCC ATACCAGCCC TCAATAACCC CCTCTTCTAG ACTCCATGAG 1320
GACCTGTAGC CCAGACCCCT GATCTGCATG GCGCCTCTGG GGTCTTTCCA GAGGTGTATG 1380
TTTTAACCAT 1390
|
