| Tag | Content |
|---|
EnhancerAtlas ID | HS105-11519 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr10:102995500-102997640 |
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 | | ZNF740 | MA0753.2 | chr10:102995509-102995522 | GGGGGGGGGGCGC | - | 6.1 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH10I101236 | chr10 | 102996521 | 102996570 | | GH10I101237 | chr10 | 102997381 | 102997510 |
|
Enhancer Sequence | TGTGTGTTGG GGGGGGGGGC GCGGTGTGGG GGGAGAGTCT GGTTCTGTTC CTGATGGAGG 60
TGGCATTTGA GTTGAACTTT GTAAAACCAG GAGCATGTAA ATAGGTGCAG GAGCAGGGAC 120
CATCCTGGAG GCAAAGGGAA CAGCCGAGCA CAAGCCCGAA GATGCCACCC TAAGAGAGGT 180
TCCAGAGTTC CCTATAGCTC CTCCCTCTGT TGTCCTGGCG GTGAGCTACT GGGTAAGGGT 240
GAAACCCTTA GTCTCTTGTT TATCGGCAGC AGGTCTGCAG CCTAGAGCCA GGGGCTGCTG 300
GACTCCTGGG ATGGCTATTT ACTTATTTAT GGGGTGGGGT GAGGGGTGGG GATGGGATGA 360
GAGAGGCTGC TTTCCTGGGC CTACAATTGG AGTTCCCTTC TCCTTGCCAT CCCCAGAAAC 420
TCCAAGAGCT GACCCTCTGT CTTACTAACT CAAACGGCCC AGAAACATCA AAGTCTGACC 480
AAAAACCGTT AATGGTAGTC AGCTCCCTCC CTTTCACAGA GGTCTCACTA CTGTCGGGGG 540
GCGCCGGGCG CAGGCCGGGC ATGGGGCCTG AGCTTAGGCC AGGTGGAAAG GTGGAAGGAC 600
CTAGTGGGGA CAGACGAAGA GACCGAGGAG CCGCCCGCCC GGCTAAATGG ACACAGGAAA 660
GGCCTGAGTC AGGCTTCTCA TAATAAATAA ACTGCACGTG AATAATTCAG CAGTCGCGCG 720
GGGGCCGGTT GCATCAGCGC CGCCGCCGCC GCGCGGCGCC CAATTCCCCG CGGAGGGGAG 780
TAGCCAATTA AGGCACTTGA AAAGGGAGTC GGGTGGAAGA TCCCCCGCCC ACCAGTATCC 840
TGGATTTACC CAGGTCGAGT TCAGAGAGCC TCCCCGGTCC CAACCCCCTC GGGCCCCATG 900
GGTCAGGGGG CCGCCTGCTG GGAAGTGCTA CCTCAGCTAA GCCGCTCAGG TGTCCCGAGA 960
CTCCGGGCAA GGGAAGACAG GCGGCGAGAC GGAGCCAGAA TAAGGGATGC GGACGTCTGA 1020
CCTGTGGAAA ACCCAGCATC TGCAGTGCCC AGCCGCACAG GGAACGTGGG CGGCGTGGTT 1080
CCAAGCACAG TGAAGACGCC AGGCTCGGAT CTGTGCTCAG AGCCGGGATC CCTCCGGGCT 1140
GCTTCGTCCT GGCCAGGACT TTCCTTGCCC TGAAGTGAGG CGCCAGGGAA GCTGCAGGGC 1200
CCTCCGCCCT CTCTGAACTC CCACGTACTT GGGCCTCTCC CAGCCTTTCT TGGACCTGTG 1260
GAAGCAATTC CTGCAGGACC AGACTCCCCT GTCTCCCCGC GGCCCCCTAG GTACACTCCG 1320
TAACTTCCGA AACCTTATTT CGTTTGAGCG AAACCCGGCC CCTTTGGCTC TTCCCACTTC 1380
CCACAAGTCC CTGGGTTCCC GATCCTGAGG GATTGCATTC ATCCCATCTC ACACCCACCA 1440
ACGCTCAATC CCTCCAGTTC CTCCCCAGCC CCTTCACTTC CATTAATTAG GTCGACTCCC 1500
TTCCTTCGCC GCTCCCTCCT GTCCCCACTC AGCCTCCCTA CACCTATGCG GCGAGCCTCG 1560
GGCCAAGACC TCCGCCCTGG CTCCGCCAGT CCTGCGGGGG CCGGCATGCA CCAGACCTCA 1620
AAAGGGATCT TCACGGGAAT TCCGCATAGC CAGATCCCAA GCCTCCAGGG AGGCCACCAG 1680
CCCTCCCCCA TCTTCTTCTT CCTCCTCCGT CTCCTTTCCT CTTCCCTCCG CCTCTACGTA 1740
TTTCTTTCTA TTCGTTTCTT TTCGTTTGGT GAGGTGCCAC CCGCCACAGC CCTGTCCCCT 1800
AGGGAGAGGC CTGGACTAAC TTTGCCGTCC TCGTGGCCTT AGCCCGGACT GTGAGTCTCG 1860
AGCGGCTTCC GAGAGGCAGC TCGGGTGTCT TCGCAGAGAC AGATGAGGTG GGCTGGCGAT 1920
TCCCTAGCCT CAGATGGCTC TGCCACCAGC CAGCTCTGTG ATCCTGGGTA AGTCTTTCAA 1980
CCTCTCTGAG TCTTGACGTT GGTAAAAGGC AGGAGATTTA GAGAAGGTGT TGGGAGACTA 2040
AATCTTTTCA TTCGTTTGAG AAAGGGAGTC GCCTGTGTTG GGACCTAAGG AGGAAGTGAG 2100
GTTCTTGAGA ATTCTAGATC TGAAATGGCC GTTTGTTTTA 2140
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