| Tag | Content |
|---|
EnhancerAtlas ID | HS050-29999 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr17:73551500-73552120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6 | MA0463.2 | chr17:73551858-73551874 | AGTTCCTGGAAAGCAT | - | 7.25 | | BCL6B | MA0731.1 | chr17:73551856-73551873 | TCAGTTCCTGGAAAGCA | - | 6.57 | | STAT3 | MA0144.2 | chr17:73551570-73551581 | TTTCTGGGAAG | + | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23798 | chr17:73551444-73552902 | Colon_Crypt_2 | | SE_28701 | chr17:73551300-73554667 | Fetal_Intestine_Large | | SE_41669 | chr17:73551532-73552852 | LNCaP |
|
| | 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 |
| GH17I075555 | chr17 | 73551481 | 73554876 |
|
Enhancer Sequence | CACAGTGTGT GTGTGTATTC TGTAATAAAT GAAAAAAACA CGTATGTGCA ACGACACTCC 60
AGGAATTCCC TTTCTGGGAA GATGGTTGGA ATTTGGTGAC AGTAAGAGTC TGTGAGACCC 120
AGCTGACTGG GGCCTGGAGG GACCTGGAAG AGCCCAGAGC AGGGCAGGGC CTCCGCGGTA 180
CTCTAGGCCC CTGGGTGAGC CCGGAGCTGC GGTGCAACCA AGATTTTCTC CCGAGAGACC 240
GGTGTCTCCA TTGTTCCAAA CTCCCCCTAC TTTCCCCACC CCACACCCAT AAGGCCCCCA 300
TGCCACTGAG GAGGGCTGGG TCCGTCACCC AGGGTGCACG TGGTGGAGGC ACCGAGTCAG 360
TTCCTGGAAA GCATTGAGAG GCTGGTATGG TGTCGGGGAA GATCAGCTCG CAGGGGTGGC 420
CATGAGGCCA AGGGCAGAGT CACAAAGGGA CAGGGGGTGG GGCCTGGTAA ATATGGGTTA 480
GGCTCCAACA CTCAGGTGTC TGGGAGGAAC CGGAAAGGTA CCGAAGCCCT GCTTCCTGCT 540
GGGTCGTCTG GTGCTGCAGC TGCAGCAGCC ATGGTGGCGC GAAGGGGACA GGTCTGCAGG 600
CCCACCCCAC GTGCTTCTCG 620
|
