| Tag | Content |
|---|
EnhancerAtlas ID | HS180-13432 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr13:47241990-47242880 |
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 | ATACCCGAAG AGGAGTACCG ATAGTATTTT GGTGTATTTC CATTCTGTCT GTCTCTCCCC 60
CTCACATACA CAGATACATG CATGTCTATA AATACACTCA CACAGGAACA CAGCTTCTGA 120
AACTTTATGC ATGTGTGTGC AAACACACAG CAGTTTTATT AAATAGTTAC ACTGAATGAC 180
ATACAGATTT TTAGATATTT CACTCTGTGG TTGTTGGCTT CAACACCAGA AGGGCAGAGA 240
AAGAAAGGGA AACTGAAACC CATCTGTCTT TTTGCTTGGT AGCAGGAAAA AGGGGCTTTT 300
TGTGGGGGAG GAGATTGAAA TAAATGGCTG ACATATAAAT AAGGATGGTT CGTAGATTTT 360
ATTTATCTAG TATTTTCCAT CTCCATGAAA ACTAAGCATT GATGATAGAA AGTTCAGAAA 420
CTTCTGGGTA GAGACCCTCT TCTTGTAGAG CAGAGATGAG ACATCAACTT AGACTTTTTT 480
GGCTGCTCTG TGGAACTAAA CCCCTCTGGG CTGCAGTTCC ACTTTGCCAG AAGACCAACT 540
TTCCTTTCTT TCTCTTTTAG TTAGCTCTCT TGCAGATACC AAAACAGACT TAAACTGTAG 600
CAACCCTTGT TTTAACAAAA GGAAGCTGAG TCAAAATGTT GGAAATGAGC CCGGTGGTTT 660
TGTGAGTTGC AGCAAAATTA TCTTCCCCAT CCCTACTGCA ATGGATGAAA TGATGCCTGT 720
GTGGTGCTGG TTGCTTTGGT CCAGCTGAGT TTCCTGCACA CATTGTCAGG AGAGGGCAGT 780
TGGCACCAGC TTCCCGTTGC TATTGGTTGT GCAGGATGTG CTCTCCATCT GCCTCCTGGC 840
TGGCCGAGGG CTCAGCTTCT AAGTGGCGGT GGCGGGGTGG CGGGGTGGCG 890
|
