| Tag | Content |
|---|
EnhancerAtlas ID | HS108-37163 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr7:73299540-73301840 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr7:73299695-73299706 | CATGAGTCACC | - | 6.62 | | JUND | MA0491.1 | chr7:73299695-73299706 | CATGAGTCACC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_01637 | chr7:73300265-73302806 | Aorta |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 73300074 | 73301348 | | chr7 | 73300263 | 73301508 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I073885 | chr7 | 73300090 | 73301975 |
|
Enhancer Sequence | TGAGTAGCTG GGACTACAGG CAAATGCCAC CATGCCTGGC TAATTTTTGT ATTTTTAGTA 60
GAGACGGGTT TTCCCCATGT TGCTCAGGCT GGTCTTGAAC TCTTGGCCTC AAGTGATCCA 120
CCCACATCGG CCTCCCAAAG TTCTGGGATT ATAGGCATGA GTCACCATGC CTGGGCTCTT 180
TTTTATTTTT TCTTTTCATT TTTTATAAAA ATAGAGACAG GGTCTCACTC TGTCACCCAG 240
GCTGGAGTGC AGTGGTGCAA TGATAGCTCA CTGCAACCTC TGCCTTCCAG GCTCAAGTAA 300
TCCTCCCACC TCAGCTTCCT AAGTGGCTGA GAGAACAGGT ATGTACCACC ACGCCCGGCT 360
AATTTTTAAA TTTTTTTGTG GAGATGGGGT CTCACTATGT TGCCCAGGCT GATCTTGAAC 420
TCCCAGCCTC AGGTGATCCT CTGGCCTCAG CCTCCTGAAG TGTTAGGATT ACAGGCGTGA 480
GCCCCCATGC CTGGCCTGTT ATTATTTCTA TGGACATGTG TTAAGCTCTA AGTCAGTAGT 540
TCTCAAACCT GAATGTGTGT GAGAATCCCC TAGAAGTCTT GTTAAAACAG ACCACTGAGG 600
CTGGGCATGG TGGCTCACAT CTGCAATCCC AGCACTTTGG GAGGCTGAGA TGGGAGGATG 660
GCTTGAGGCC AGGAGTTTTA GACCAGTCTG GGCAACATAG AGAGACCCTG TCTCTACAAA 720
CTATTAAAAA AATTAGCCAA GTATGGTGCA TGCCTGTAGT CCCAGCTGCT CAGGAGGCTG 780
AGGTAGGAGG ATCGCTTGAG CCCAGGAGTT TGAGGCTGTG GTAAGCTATG ATTGCACCAC 840
TGCACTCCAG CCTGGGTGAC AGCGCAAGAC CCAGTCTCCA AAACAAAAAC TACAAAAACA 900
TAAAACAGAC CACCGGGTGT CATTTCCAGA GTTTCTGATC CAGTAGGTCT GGGCTGGGAC 960
TGATAATTTG CTTTTCTAAC AAGTTTCCAG GTGATATGGA GCTACTGGTC GGGGGCCACA 1020
CTTGAGAGCT GATCTCAGTC ATTATCAGCT ATTAACACCC GTGTGTGGAT TAGCTTATCA 1080
GACCATGGAA ACCAAAGACT TCCTCCCACA AGGGAGGTCT GGACAGAGTA AGGCTTGTGG 1140
AAGGACCAGG GCCTTGGGGG TGAGAGAGGA AACATTGCCA AGAGGCAGAC AGAGGCCCAG 1200
AGGGCTGTCT GGCGGCACAG AGGACAGGCT TTGTCTTTTT CCTAGGCTGG GCAGGACCCC 1260
AGAGGTTAGG CTCTGGGACA GGAGGGAGGC GGGCAGGCCT GGGGAAGTCT GGGCAGCCCG 1320
TGCTGAACAG AGGCTGGGAT CGGGCGGTGG GCCCGGTGCA CCTGACCCGC GGGGCTGGGA 1380
ACAATGGCTG GGCCGGCGTG GCCTGGCTTG CTGCCCCTGT TCATCTCTGT TTTCCTTCCC 1440
AGCTCCGATC TTCGCCGGCT CTCCTCACTC GCTCCCTCTC CGGCGGCCCA TCCTGTCCGC 1500
TGGCCCCCAG ACAGCACATT CCTTCATGCT GATCTCTTCC CGGTGGCTGT GAGTGCACGT 1560
TCTCACAGCG AGGCAGGGAC TGGGGCCATG AGGAAGGGGG GCTCAGGTGG CCTTCCTGGG 1620
GGCCCTGGCC CCACATCCGG AGACCAGAGG GCACCTGGAT GGGAAGGAGG AATAACCCCT 1680
CAGGCTCGGA GTCCTCCAGG ACTCAGCTAG CCCTGAGGAT TTGGATCATT TCCCCCCCAG 1740
TCCTTCATCT CTTGATATTA GGAGGTTGGG GGGTCCTGCA CTGCTAAGCC TCCTAGCCCT 1800
GTGCCCTGGT GTGGTGACCG AATTGGCTGT ATCCTCTGCA GAGCATGGCC CCTGTCCAGT 1860
AGACTCAGGA CATTTTCTGC TTCTCATGGG GGCAGTGGCC CAATGCCAGG CTTTCCTTGG 1920
TCCCATCTGG GCCAGGACCT TCCCCTGGTT TCATCTCCCT TCCTTGAAAG ACCCATCTGC 1980
AGCAGCGTGG AAGGATCCAG GCCCCCTCTG CCAGCCTTTC ATTCACCCAC GCAGAGGCAG 2040
GCAGGCTGTG CAGCCCCCAC CCCACAATTT GATAAGCCTG AGCCAGGGAG GGCAGGGCTG 2100
GCCAGTGTGA CAGCTCATGA GTGGCCGGTA TCCTCTCTTC CTCTCCGGTA CCTGGTGGCC 2160
CCAGTCCTGC TGCCCTGCCT GGCAGCAGAG GGGATGGGCT GGTGTCTGCT GTCCTGAGAG 2220
CCTTTCCTGG GCTGTCTGTA CTGGGTCAAG GCTCTGCCTT GGGGTCAGGT TTAGTTTGAG 2280
GTCACGGTGA GGATCAGGGC 2300
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