| Tag | Content |
|---|
EnhancerAtlas ID | HS182-01649 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:183536480-183538270 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr1:183537565-183537577 | TGCTGTGATTTC | - | 6.22 | | Gfi1b | MA0483.1 | chr1:183537565-183537576 | TGCTGTGATTT | - | 6.62 | | Sox3 | MA0514.1 | chr1:183537692-183537702 | CCTTTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_53951 | chr1:183536043-183538665 | Spleen |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 183536694 | 183537136 | | chr1 | 183537727 | 183538062 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I183567 | chr1 | 183536380 | 183539055 |
|
Enhancer Sequence | CTGCAGAGGA TAGACACAAG ATCCAGCCCC CATCCCCTCA CATGATGCCA TGGCGCAAAT 60
ACACTGAACT TGGAGCCAGG GACTTGGCTC CAGCCTGGCT CTAACTCCAC ATCTAACTGC 120
AACTGCCGAG ATGACACTGA GCCTGCCTGG GCTCCCAAGA GGTCTCAGCA AGAAACTGGT 180
GTACACCTGC TCATAACCAT ATATGCAGAG GGGCAAGAAT AAAGCAAAAA CCCCACAACA 240
CTAGATAGTG AGGACTTACA ATCCTTGCCC TCCCTTCTGC TCTGAGGAGG AAGGTCCCTG 300
GCTGTGTCAT CTTGGCCAGC ACCCAAGGCT GGGCTGGGGT GGGGTGGATC AGGTGACTGT 360
GGTCAGGGGA ACAGCACAAA GCAGAAGTCA GGTGAGAGCC AGCTGGGCCA GAAAGATTGG 420
TGGGAGAGGA GGAAGGAGAA ACCACCTAGA ACCAGTGTTG GGCCAGGATA GAGAGACCGT 480
GAGCAGGGTA GGTGACAGGG AGCGTGAGGG ATGCACATAG AGGGCTCTGA GGCTGCCCAG 540
CTGCCGTGGT GCAGTGTCGG TTCCCTTAAG TCTGACTTCA TGCTTTTAGG CTTTGAGGCT 600
CTGATTGGCA TCACTTTGGA ACGTGTGACT GAGAGGCTGG TGTTCAGGTT TCAGGCTTCC 660
CTCCCTTTAC TCCCCACTCT GTTACTTTCC CCTCGGCCCA TCCTTGTTTC CAGACATCGT 720
GCCTACTCCT GTAGGGAATA CAGGCCCTTC CAGCTGACAG GGAGCTTAGG AATGAGCTCA 780
TCCAGCCCCC TCATTTTTGT AGTTGCTTTG GTACTTTTGT CACTTTTTTT TTTTTGAGAC 840
GGAATCTTGG TCTGTTGCCC AGGCTGGAGT GCAGTGACAT GATCTTGGTT CACTGCAACC 900
TCCACCTCCT GAGTGCAAGT GAGCCTCCTG CCTCAGCCTC CCAAGTAGCT GGTATTACAG 960
GCACATGTCA GTCACCACAC TCAGCTAATT TTTTCATGTT TAGTAGACAT GGGGTTTTGC 1020
CACGTTGGCC CGGCTGGTCT CGAACTCCTG ATCTCAAGTG ATCCGCCCAC CTCAGTCTCC 1080
CAAAGTGCTG TGATTTCAGG CATGAGCCAC ACACCTGGCC AATCACTTTT TAAAACCTCC 1140
TTTTTGGGTG GGAGGACCAG GCTTGCTTCA TCACTTTGAG AGAATTCTTA AGAAAGCTGT 1200
AGGTTATGTC ACCCTTTGTT TTTCATCTTA CAGAAGAAGG ACTTCCTTTT CTTCAGTCCT 1260
TCCTCTTTAC TTCTTCAGAA AGCATGTGCC GATAGGGAGT GGAAAACATC CACACAGGAA 1320
AAAGGACGTC ATTCTAGATT CCTGACTCCA GAGAGCTCTG GCCTGCCCCC GTCAGAGGGG 1380
ACTGCAGCCA GTGCGAAACC GATCTCCAAC CTGAGGTCAG CATCCTGGTC CCCAGGGTAG 1440
CTATGTTCCA CAGAACACCA CTGCCCCTCA GCAACAACCC CTTGCCATGT GGGTGGCTGT 1500
GCACGTGGAC AGAGGGCCAA TGGGACACCA CGTAGCTGCA GCCAAGCCCT GATGGCCAGC 1560
CCCACCACAG TCAAGACTCC CATCCCCATC ATATCATTCC TTTCTAGCCT GACATTCTAG 1620
AAGACATTCT TCTAGGCATT CCTTTCTAGC CTGACATTCT AGAAGAAGCC TGACATTCCA 1680
GAAAATTCAA CAAGATTTAG ACCCTGACCC CACCTTCATC TTCTTCCCTC CCTTTCTTGC 1740
CATCAGCTCA GGCTTGGCGC TTGGATATTC TATTTATGGA TTTGAATCTA 1790
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