| Tag | Content |
|---|
EnhancerAtlas ID | HS073-09474 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr21:30718900-30720280 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr21:30719774-30719789 | GAAGTACAAAGGCCA | + | 6.15 | | MEF2C | MA0497.1 | chr21:30719423-30719438 | AGGCCAAAAATAGCA | + | 7.19 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09591 | chr21:30718198-30722156 | CD14 | | SE_45766 | chr21:30710260-30724545 | Osteoblasts | | SE_56659 | chr21:30717773-30721301 | u87 |
|
| | 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 |
| GH21I029346 | chr21 | 30718745 | 30725019 |
|
Enhancer Sequence | GGACACTTGG CAGTTCCCAG AGACACAAAT CTCGGGGGCA GGGTATAGGA TATGGCTTCT 60
AGGGGCAGAG GCCAGGACAG CCCTCACAAC AATTACCCAC CCAGGGTATC GATCTGGCTG 120
ACATTGAGAA ACCCTGACTA GACCAACGAT GGAATCAAGA TGACTTGTAA GAAAGTGCTC 180
AGTTGTGTGA GATAGTGTGG TGGCTGCAAG AGTTCAAAGG AGACAGGGTG AGAAACGTGG 240
GATTTCACCA AGCTTTGAAA GATTGTAGTC TGAATCGGGA GAAGATGGTC TCTGGGGAGA 300
GGAGGCCACT TGGCACAAAT AAGCCTGGCG TGTTAAAGGA ACAGAAGGAG GTTGTCACAG 360
TGAGAGGGAG AAGGAGGAAG GCCCCCACTT GAGTGTTCAC CAGTGGGTGT CCCAGCATCT 420
TGCCCTACCC AGATTGACTT AAGTTATCGA AGGTCTGAGG TTAGACTGTA AGGGCTTTAA 480
GAGCAACAGA AGTATAGGTA GTAGGTATTG AGGGTTTAGA GGAAGGCCAA AAATAGCACC 540
CTTTCCCTGG CCAGAGTTTT GAACCATTTG AGAAATAAAA AGTAGGTGAA GTCCATATCG 600
CTGATGGAAC CCAGCTTGGA ACCATGGCTT TCTAGCTGTT TAGCCCAGTG AACCTGCTAA 660
AAGTGCATTC TGGAATTAGG CAGACTTAAT CCATCCACCG GTCACCTTGG ACGACCCCAA 720
AAGGGGCAGA GCTCTTAGAG GAGCAGAAAA ATGTAAACAG GGAGCAAATT CCACAAGTAA 780
GGGGTGGGCC GAGCCAAGTA GACTTAATGA CGCTAAAAAT TTACTCATTA GAATCAGGGA 840
CTACTACATC AGGGCCAGGA CAAAGTACAA AGTGGAAGTA CAAAGGCCAG AGGGTGTTTC 900
TTGCCCTGGA GATTTAAACT AGGGAAGTCT TAGGGAAGAG TGTTCCCCTT TCATGCTCCC 960
CAGTTTAAGT TCTCTTGAAA CATTGGCCCA TTGCTCAACC AGGGCTGTGA CTGATGGCCT 1020
GGAGGAGGAG AGCATCTGTT CCAGAGGGCA GACCTCCTCT CACCTTTGAG GCCACTTCCC 1080
AACACCAGCC TTTGCAGGTG TGACTGGCTT GGGCTGTCAG TGAACATTTG GTCTCAGAAG 1140
GCTCTGGATC CAGCAGTGTA CTAGTAAGTA AATGAATTCA AAGGCTACTC TGTACCAAAG 1200
ACTGAACATT TTTCTCATCC CTAATTCTCT CCTACCTCAT CGTCCCGTGT AGCATGTAGC 1260
ATATCAGATG TTCTGCATTG AGATTAGATC CCAACATAAC ATTCCCATAA GAAAATGCAT 1320
GAAAGTCCAG GAATAAAATG CTAGCAACAT AATGATATCC AAATTTGAAT GGAAGTTTAA 1380
|
