| Tag | Content |
|---|
EnhancerAtlas ID | HS193-09153 |
Organism | Homo sapiens |
Tissue/cell | U87 |
Coordinate | chr13:47241920-47242890 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr13:47242532-47242553 | CCTTTCTTTCTCTTTTAGTTA | + | 6.09 | | IRF1 | MA0050.2 | chr13:47242227-47242248 | AGAAAGAAAGGGAAACTGAAA | - | 6.74 | | IRF1 | MA0050.2 | chr13:47242233-47242254 | AAAGGGAAACTGAAACCCATC | - | 6.97 | | IRF9 | MA0653.1 | chr13:47242235-47242250 | AGGGAAACTGAAACC | + | 6.02 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_14324 | chr13:47241650-47242893 | CD34_Primary_RO01549 | | SE_26329 | chr13:47241821-47242908 | Duodenum_Smooth_Muscle | | SE_30455 | chr13:47241764-47243668 | Fetal_Muscle | | SE_54689 | chr13:47241818-47243170 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr13 | 47242087 | 47242800 | | chr13 | 47242224 | 47242549 | | chr13 | 47241928 | 47242851 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I046664 | chr13 | 47238537 | 47243788 |
|
Enhancer Sequence | AAGCACTTGT AGAAAGTTTG GAAAATACAT CAAAGTATAA TAATGGAAAT AAAAACCATC 60
CATTGTACCT ATACCCGAAG AGGAGTACCG ATAGTATTTT GGTGTATTTC CATTCTGTCT 120
GTCTCTCCCC CTCACATACA CAGATACATG CATGTCTATA AATACACTCA CACAGGAACA 180
CAGCTTCTGA AACTTTATGC ATGTGTGTGC AAACACACAG CAGTTTTATT AAATAGTTAC 240
ACTGAATGAC ATACAGATTT TTAGATATTT CACTCTGTGG TTGTTGGCTT CAACACCAGA 300
AGGGCAGAGA AAGAAAGGGA AACTGAAACC CATCTGTCTT TTTGCTTGGT AGCAGGAAAA 360
AGGGGCTTTT TGTGGGGGAG GAGATTGAAA TAAATGGCTG ACATATAAAT AAGGATGGTT 420
CGTAGATTTT ATTTATCTAG TATTTTCCAT CTCCATGAAA ACTAAGCATT GATGATAGAA 480
AGTTCAGAAA CTTCTGGGTA GAGACCCTCT TCTTGTAGAG CAGAGATGAG ACATCAACTT 540
AGACTTTTTT GGCTGCTCTG TGGAACTAAA CCCCTCTGGG CTGCAGTTCC ACTTTGCCAG 600
AAGACCAACT TTCCTTTCTT TCTCTTTTAG TTAGCTCTCT TGCAGATACC AAAACAGACT 660
TAAACTGTAG CAACCCTTGT TTTAACAAAA GGAAGCTGAG TCAAAATGTT GGAAATGAGC 720
CCGGTGGTTT TGTGAGTTGC AGCAAAATTA TCTTCCCCAT CCCTACTGCA ATGGATGAAA 780
TGATGCCTGT GTGGTGCTGG TTGCTTTGGT CCAGCTGAGT TTCCTGCACA CATTGTCAGG 840
AGAGGGCAGT TGGCACCAGC TTCCCGTTGC TATTGGTTGT GCAGGATGTG CTCTCCATCT 900
GCCTCCTGGC TGGCCGAGGG CTCAGCTTCT AAGTGGCGGT GGCGGGGTGG CGGGGTGGCG 960
GGGGGACTTT 970
|
