| Tag | Content |
|---|
EnhancerAtlas ID | HS010-02031 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr18:21442120-21442910 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr18:21442770-21442784 | AGTCCCCTGGGACT | - | 6.32 | | EBF1 | MA0154.3 | chr18:21442770-21442784 | AGTCCCCTGGGACT | + | 6.57 | | IRF2 | MA0051.1 | chr18:21442158-21442176 | GGAAAACGAAAGCTAACA | + | 6.69 | | NEUROG2 | MA0669.1 | chr18:21442378-21442388 | GACATATGTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35820 | chr18:21440540-21443393 | HMEC |
|
| | 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 |
| GH18I023860 | chr18 | 21440821 | 21446901 |
|
Enhancer Sequence | AATTCTTTAT TTTAAGGCAG AAGAAAGCCT CTTTGTTAGG AAAACGAAAG CTAACAAGTG 60
ACTCACAAGC TTATTAAAAG AAACACAGGA TCTGGTGGCA GTTCGACTTT CCTAAGTAGA 120
ATCACATAGT TACACACTCC TCAGGAACTT ACAAACCACT TGCTCTTCCT TTGCTGCAAG 180
AGTTATTATG CCAGAGGCTG GCCACCTCCA TCCATTTTAT GAGGACAGAA ATGCAGGCCT 240
CATGTGGAAA CATGAGGTGA CATATGTTTC TTAGCAAGGG TGGAACTTGC TAACGGGTGG 300
ATTTCACAGG GCCTGGCTCA GGGGATGCCA AATTCTCACA TTAGGAAGAC TAAAATAATA 360
GGGCCTTGTT GGCCTGAGGT CTCTAACTTT GTCTTCTGGG TGAAGGACTG TGGGTTTTGA 420
CATCTGAGTG TGGGAAATGT TGCCTCTCTT CTATGATCCC ACTTCTCTTT CACTTAATAC 480
TCCTCTTTAC CGCTATATGA CGGGCCCATG TGTTGATTAT CTATTGCTAT GTAACAAATT 540
ACTCCAACAC TTCGCAGCTT AAAGCAGTAA TGATTATCTT GGATGAGGAA TTCAGGAGGG 600
GATGGCCCAG AGTCTTCCTA GGTTACTGTC AAGATGTCAA CCAGGGCTGT AGTCCCCTGG 660
GACTGCAGCA TCTGCTTCCA AGCTCACCCA CATGGCTGTT AGCAGGCCTC TGCTTCTGGC 720
TAGCTGTGGG CTGGAAGCCT CCATTTCTCA TCACGTGAGA CCCTCCATAG GCTACCTGAG 780
GGTCCTCATG 790
|
