| Tag | Content |
|---|
EnhancerAtlas ID | HS060-09408 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr13:47242010-47242880 |
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: 2 | Chromosome | Start | End |
| chr13 | 47242087 | 47242800 | | chr13 | 47242224 | 47242549 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I046664 | chr13 | 47238537 | 47243788 |
|
Enhancer Sequence | ATAGTATTTT GGTGTATTTC CATTCTGTCT GTCTCTCCCC CTCACATACA CAGATACATG 60
CATGTCTATA AATACACTCA CACAGGAACA CAGCTTCTGA AACTTTATGC ATGTGTGTGC 120
AAACACACAG CAGTTTTATT AAATAGTTAC ACTGAATGAC ATACAGATTT TTAGATATTT 180
CACTCTGTGG TTGTTGGCTT CAACACCAGA AGGGCAGAGA AAGAAAGGGA AACTGAAACC 240
CATCTGTCTT TTTGCTTGGT AGCAGGAAAA AGGGGCTTTT TGTGGGGGAG GAGATTGAAA 300
TAAATGGCTG ACATATAAAT AAGGATGGTT CGTAGATTTT ATTTATCTAG TATTTTCCAT 360
CTCCATGAAA ACTAAGCATT GATGATAGAA AGTTCAGAAA CTTCTGGGTA GAGACCCTCT 420
TCTTGTAGAG CAGAGATGAG ACATCAACTT AGACTTTTTT GGCTGCTCTG TGGAACTAAA 480
CCCCTCTGGG CTGCAGTTCC ACTTTGCCAG AAGACCAACT TTCCTTTCTT TCTCTTTTAG 540
TTAGCTCTCT TGCAGATACC AAAACAGACT TAAACTGTAG CAACCCTTGT TTTAACAAAA 600
GGAAGCTGAG TCAAAATGTT GGAAATGAGC CCGGTGGTTT TGTGAGTTGC AGCAAAATTA 660
TCTTCCCCAT CCCTACTGCA ATGGATGAAA TGATGCCTGT GTGGTGCTGG TTGCTTTGGT 720
CCAGCTGAGT TTCCTGCACA CATTGTCAGG AGAGGGCAGT TGGCACCAGC TTCCCGTTGC 780
TATTGGTTGT GCAGGATGTG CTCTCCATCT GCCTCCTGGC TGGCCGAGGG CTCAGCTTCT 840
AAGTGGCGGT GGCGGGGTGG CGGGGTGGCG 870
|
