| Tag | Content |
|---|
EnhancerAtlas ID | HS038-11042 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr2:33439480-33440600 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EBF1 | MA0154.3 | chr2:33440139-33440153 | ACTCCCTGGGGAAT | + | 6.19 | | EBF1 | MA0154.3 | chr2:33440139-33440153 | ACTCCCTGGGGAAT | - | 6.49 | | RUNX1 | MA0002.2 | chr2:33440548-33440559 | TTCTGTGGTTT | + | 6.32 | | TCF3 | MA0522.2 | chr2:33439998-33440008 | AACACCTGCT | + | 6.02 | | TP53 | MA0106.3 | chr2:33439519-33439537 | TACGTGCCTGTGCATGTT | + | 6.2 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_01563 | chr2:33439147-33442468 | Aorta | | SE_02477 | chr2:33434729-33442418 | Astrocytes | | SE_39262 | chr2:33434086-33442297 | IMR90 | | SE_45791 | chr2:33434082-33443143 | Osteoblasts | | SE_56575 | chr2:33434080-33443505 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 33439498 | 33439559 | | chr2 | 33439613 | 33439863 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I033209 | chr2 | 33434098 | 33442502 |
|
Enhancer Sequence | TGGATCTGTC TCTCCCTCTT CTTCTCCCCA CTCTGCGTGT ACGTGCCTGT GCATGTTTGT 60
TTCGTCATCT CTGTGACTAC CTACCCACCT ACCACTTTAT CACTCTTTTT TTGGTCCAGT 120
CTTCCCCCGT GTCTGAGACT GTTCATCTGT GGCCCTGCCG CTGTTCCAAC CTCGGGGACT 180
TTCCCTCACT GCACGTGGTT AAACACTTTG CTGAGAGCCC TGTCTTCAAA CAGACTTCCC 240
CAGGTCATTG TGTTGGTATC TGGCACACAA CGTCACTCAT TGTTTATCCA GTTGTGTTGT 300
TTTATAAGAG AGTTTCTTTA TCTCAAGGAA TGCGTGTCAC GTGTCTGCAG GAGTTACTGC 360
CCCGGTTTCA AGAGATGTGA TGGTCTTGGG CTTTACTGAC TTACACTAGG GCTTTTTTCA 420
GTGCCTTCCC CAGAATTACG TGTTTTTTCA AGTTCATCTA AAAAAAAAAA AAGCAATTGT 480
TTTGGTATGC CTAGTTTTGC TTAACTCAGA ATGTCTTTAA CACCTGCTTT TATATTAGGG 540
AAGTTCATTT TGTCTCGTAG GGTCGTTTCT TATGGAGTCT GGTACTTTCG AGAGGGCAAT 600
TAGACTAACC TGTTTGATTG ACAGGACCGT TTACAATCTA CTCCACTCAC ACGCCTTCTA 660
CTCCCTGGGG AATCCGACAA ACATTTGGGG CCTCAAATGG GACATCTGGA GTAGGGAGCT 720
TTTATCTATA ATAATAATAA TAATGATAAT GGTAATGATA GCTGACACAT GTAAGTGCTC 780
AGCTATAATG TTCAGCATTG CACATGCCTT TTTTCTTTCA TGTTTCATGA CCCTAGGAGA 840
AAGATACTAT TATGCACTCT ACGTTATGGG TAGGAAAATG TCTAAGATAA TGCGTGTAAG 900
AAGTCCTACA GTCAGAATTC ATTCTCAGGC CTCTCTAACT CCTGAGTCAC ATTTTTAATC 960
ACTATCATAT ACTGCTGTTG GAGAGCACAC AGCATCCTGT TGAAATCATT AAAAATAATA 1020
AAACCTTAGA ACATCAAAGC TATGATGTAA CTAAAACTTA GCTGAGCCTT CTGTGGTTTG 1080
GTCTTGTTTT ACAATTTGGA TATGTAGTTA CTTAGCGCCT 1120
|
