| Tag | Content |
|---|
EnhancerAtlas ID | HS092-07524 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr10:102995570-102997690 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| PLAG1 | MA0163.1 | chr10:102996383-102996397 | CCCCCTCGGGCCCC | - | 6.65 | | ZNF263 | MA0528.1 | chr10:102997196-102997217 | TCTTCCTCCTCCGTCTCCTTT | - | 6.46 | | ZNF263 | MA0528.1 | chr10:102997193-102997214 | TCTTCTTCCTCCTCCGTCTCC | - | 6.4 | | ZNF263 | MA0528.1 | chr10:102997184-102997205 | CCCCCATCTTCTTCTTCCTCC | - | 7.44 | | ZNF263 | MA0528.1 | chr10:102997187-102997208 | CCATCTTCTTCTTCCTCCTCC | - | 7.91 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH10I101236 | chr10 | 102996521 | 102996570 | | GH10I101237 | chr10 | 102997381 | 102997510 |
|
Enhancer Sequence | GTTGAACTTT GTAAAACCAG GAGCATGTAA ATAGGTGCAG GAGCAGGGAC CATCCTGGAG 60
GCAAAGGGAA CAGCCGAGCA CAAGCCCGAA GATGCCACCC TAAGAGAGGT TCCAGAGTTC 120
CCTATAGCTC CTCCCTCTGT TGTCCTGGCG GTGAGCTACT GGGTAAGGGT GAAACCCTTA 180
GTCTCTTGTT TATCGGCAGC AGGTCTGCAG CCTAGAGCCA GGGGCTGCTG GACTCCTGGG 240
ATGGCTATTT ACTTATTTAT GGGGTGGGGT GAGGGGTGGG GATGGGATGA GAGAGGCTGC 300
TTTCCTGGGC CTACAATTGG AGTTCCCTTC TCCTTGCCAT CCCCAGAAAC TCCAAGAGCT 360
GACCCTCTGT CTTACTAACT CAAACGGCCC AGAAACATCA AAGTCTGACC AAAAACCGTT 420
AATGGTAGTC AGCTCCCTCC CTTTCACAGA GGTCTCACTA CTGTCGGGGG GCGCCGGGCG 480
CAGGCCGGGC ATGGGGCCTG AGCTTAGGCC AGGTGGAAAG GTGGAAGGAC CTAGTGGGGA 540
CAGACGAAGA GACCGAGGAG CCGCCCGCCC GGCTAAATGG ACACAGGAAA GGCCTGAGTC 600
AGGCTTCTCA TAATAAATAA ACTGCACGTG AATAATTCAG CAGTCGCGCG GGGGCCGGTT 660
GCATCAGCGC CGCCGCCGCC GCGCGGCGCC CAATTCCCCG CGGAGGGGAG TAGCCAATTA 720
AGGCACTTGA AAAGGGAGTC GGGTGGAAGA TCCCCCGCCC ACCAGTATCC TGGATTTACC 780
CAGGTCGAGT TCAGAGAGCC TCCCCGGTCC CAACCCCCTC GGGCCCCATG GGTCAGGGGG 840
CCGCCTGCTG GGAAGTGCTA CCTCAGCTAA GCCGCTCAGG TGTCCCGAGA CTCCGGGCAA 900
GGGAAGACAG GCGGCGAGAC GGAGCCAGAA TAAGGGATGC GGACGTCTGA CCTGTGGAAA 960
ACCCAGCATC TGCAGTGCCC AGCCGCACAG GGAACGTGGG CGGCGTGGTT CCAAGCACAG 1020
TGAAGACGCC AGGCTCGGAT CTGTGCTCAG AGCCGGGATC CCTCCGGGCT GCTTCGTCCT 1080
GGCCAGGACT TTCCTTGCCC TGAAGTGAGG CGCCAGGGAA GCTGCAGGGC CCTCCGCCCT 1140
CTCTGAACTC CCACGTACTT GGGCCTCTCC CAGCCTTTCT TGGACCTGTG GAAGCAATTC 1200
CTGCAGGACC AGACTCCCCT GTCTCCCCGC GGCCCCCTAG GTACACTCCG TAACTTCCGA 1260
AACCTTATTT CGTTTGAGCG AAACCCGGCC CCTTTGGCTC TTCCCACTTC CCACAAGTCC 1320
CTGGGTTCCC GATCCTGAGG GATTGCATTC ATCCCATCTC ACACCCACCA ACGCTCAATC 1380
CCTCCAGTTC CTCCCCAGCC CCTTCACTTC CATTAATTAG GTCGACTCCC TTCCTTCGCC 1440
GCTCCCTCCT GTCCCCACTC AGCCTCCCTA CACCTATGCG GCGAGCCTCG GGCCAAGACC 1500
TCCGCCCTGG CTCCGCCAGT CCTGCGGGGG CCGGCATGCA CCAGACCTCA AAAGGGATCT 1560
TCACGGGAAT TCCGCATAGC CAGATCCCAA GCCTCCAGGG AGGCCACCAG CCCTCCCCCA 1620
TCTTCTTCTT CCTCCTCCGT CTCCTTTCCT CTTCCCTCCG CCTCTACGTA TTTCTTTCTA 1680
TTCGTTTCTT TTCGTTTGGT GAGGTGCCAC CCGCCACAGC CCTGTCCCCT AGGGAGAGGC 1740
CTGGACTAAC TTTGCCGTCC TCGTGGCCTT AGCCCGGACT GTGAGTCTCG AGCGGCTTCC 1800
GAGAGGCAGC TCGGGTGTCT TCGCAGAGAC AGATGAGGTG GGCTGGCGAT TCCCTAGCCT 1860
CAGATGGCTC TGCCACCAGC CAGCTCTGTG ATCCTGGGTA AGTCTTTCAA CCTCTCTGAG 1920
TCTTGACGTT GGTAAAAGGC AGGAGATTTA GAGAAGGTGT TGGGAGACTA AATCTTTTCA 1980
TTCGTTTGAG AAAGGGAGTC GCCTGTGTTG GGACCTAAGG AGGAAGTGAG GTTCTTGAGA 2040
ATTCTAGATC TGAAATGGCC GTTTGTTTTA ACGAGTATTT TGGGAGCAGC TGATAACTTT 2100
TTATTTTTAT TTTTATTTTT 2120
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