| Tag | Content |
|---|
EnhancerAtlas ID | HS010-02866 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr21:36900880-36902210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GATA2 | MA0036.3 | chr21:36901900-36901911 | TTCTTATCTGT | + | 6.14 | | Gata1 | MA0035.3 | chr21:36901900-36901911 | TTCTTATCTGT | + | 6.62 | | IRF1 | MA0050.2 | chr21:36901640-36901661 | CTCTCCTTTCACTTTCACTTC | + | 8.09 | | Nr5a2 | MA0505.1 | chr21:36901508-36901523 | CTTGGCCTTGAACCC | - | 6.14 | | PRDM1 | MA0508.2 | chr21:36901648-36901658 | TCACTTTCAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_25514 | chr21:36899291-36903184 | DND41 |
|
| | 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 |
| GH21I035528 | chr21 | 36900499 | 36902955 |
|
Enhancer Sequence | GCTAAGCAGT TGAAAAGGGT TGAAAAAGAA AGATGTAGGT TTAGGTCCGG AGCCTGGCGC 60
ACCCGCCCTA ATTTGAGTCA GGGACCCTAG GCGCCTGCAG CTCCGGTTCG GGTTGAGTGC 120
CTCCTGTCAG GATGTGAAGC TGCTGTCCCC CCCGGGGGCC TCCAGCACTG CTGAGGACTC 180
AGCAGTCAGC CTCTCCTCCC ACTTGGGCTC ATTTACAGAG AGCATCTCCA GGAATCAGTC 240
ATGGGGAAAG GGGAAACGCG GAGTGACAAC ACAACACGTA GAAAGTTCTC TGCCGCCTTG 300
GTCAGGCTTG TCAGCCTCAC AGCCCATCCT GCTCCTGCGG GAGGAAAAGT GAGCAGAACT 360
CAGCCCGGAG ATGAGCCGCA GGCCGGCAGC CCCTGCCTCT GCCCTGCTTG TTGTGACTGC 420
AATGCAAGGC TCTCTGTAGG TGCGGGGGAT TCGGGTTAAA TGGGTCTCCA GTGGTCCAGC 480
GCTCCCAGCA AAGGCCGACC ACAAGAATTA GCGGGCTAGT TATTTACCAT AACCATATAC 540
AAAACCACAA GCATCAGCGT TCCCTCAAAT ACATCCGAGA CGCTGTATAT CTCTTTATTA 600
AAGCCTGTCA GGGTTTGTTA TTGCACAGCT TGGCCTTGAA CCCCAACTAA ACCAGGCTGC 660
TTGAGCAAAG AACCAAGCAA TGCAAGCATT CAGGCAGGAC CATTATAACC CTGAGGCCAA 720
AGGCAGAAGC AGGGAGAGGA GACGTCTTCC TCTCCTGCCT CTCTCCTTTC ACTTTCACTT 780
CGAATTGATT TTTAACTACA TTCGAGCTCA CGATGATAGA TGGCTGTAAA ATATTTTAAT 840
CATTCATAAA TAAAGTATTT ATCTTGTGTG AGTTATCCGG TCTCCTTCAC TTTAATGAAC 900
ACAGTATACA TCACGCTAAT CCATTACTAT CAATCATAGG TTTCAAGGTA GGCAATGTAA 960
AAACTTAGAA TTGTTGTCAT CCCTTCTAGG CCTTTGGACT AAGATCAGGT TTGGTTGCTA 1020
TTCTTATCTG TTTGCTTAGT TTTACTTTGC CTCGTTCTCA GACCTATTTT TTTCAAAGCC 1080
ATGATGTATG CATTCTAGCA CATTGATGTC ATTTTGAGTT CAAATGCCCC ACTGGTTAAG 1140
AAAACAGCAC AATGTGGAAT TTTCAGCTTT CAAAAAGGTC TTTGCTACAA GACAACTCAG 1200
ATAAAGAATT TAGCAATAGC CAAGATAGAG TGGTGGTGAT TAAGTGATGT AATCAAAGGA 1260
TTGCAATTCC CATTCTAAAT AACTCTCTAA CTTCAAATTT GACTATGGGG TGACCAACCT 1320
ATCGGGGTGT 1330
|
