| Tag | Content |
|---|
EnhancerAtlas ID | HS121-10411 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr13:110819580-110821970 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr13:110820365-110820379 | TTCTTCCTCTTTTT | - | 6.14 | | SPIC | MA0687.1 | chr13:110820365-110820379 | TTCTTCCTCTTTTT | - | 7.01 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH13I110169 | chr13 | 110821701 | 110821850 | | GH13I110170 | chr13 | 110821867 | 110823423 |
|
Enhancer Sequence | GACACGCAAA GAGGAGGTTG GGAATTGCTC AGGATATGTA GGTTAAGTCT CTCCAGTAAC 60
CTGCTAGTTG GAAAATGGAA ACAGCCCCTC AATGTTCTGG AAAGCACATT TGTGAACAAA 120
TGGTGCCTTG TGGTTTCTTA AATGACAGAA TAACAACACC TTTGCATGTG CCTCAATCGG 180
GAAGCTGGAA AGTAGAAGCA TTTGTTTCCC TCCCATGTAT CTCCTCTGCT TGTCCATCCA 240
CAGGGGAAGC GCCTGAGGAG CAGGCAAATG TCCTGCCCTT GCCACCTCCA GCTCACAGCA 300
CGATGCCATA GACAGAGCCA GGGCCCCCTC AACACCTGTG ACGGCAACAT AGCCATCCAG 360
CACCAGCCAA CGAGCTTTTC TGAAAACTTT CCCCTTAATC CTCAAGTGCA ATCAGTTTTC 420
TTTAGAATTA GTTTCATGTC TTATCTGAAA ACTGATTTTA AATATGCAAA GAAAATTAAG 480
AAATGCTAAG GAACGAGTAT TTTCCTTTAT ACTGTGGCAA TATTCGTGTA TTTTAAAATA 540
GGGGCTCATT TTCTTTCCAT TTCAACAAGT CGTTCCTTTC TCAAGTCGTG GACAGCAACA 600
TGTAACAAGT TGTTTTATTT CTTACGTAGA TTTGTTTCTT AGCCTTATTT TAAAAGTGTC 660
AAACCAAAAT AACATGAACA AATATATATG TATATAAACA TATATACAAA CACATATTTA 720
TACATAAGTA TGTATACAGA GACAGACAGA CACTGACTGG CACCAGGAAT GGGGTGTATT 780
TCTTTTTCTT CCTCTTTTTT TTTTGAGACA GAGTCTCGCT CTGTCATCCA GGCTGGAGTG 840
CAGTGGCACC ATCTCGGCTC ACTTCAATCT CTGCCTCCTA GGTTCAAGCA ATTCTCCTGC 900
TTCAGCCTTC CAAGTGGCTG GGATTACAGG CATGAGCCAC CATGCTAACT TGTGCATTTT 960
TAGTAGAGAC AGGGTTTTGC CATGTTGGCC AGGCTGGTCT CGAACTCCCC ACCTCAGGTG 1020
ATCTGCCCAC CTCGGCCTCC CAAAGTGCTA GGATTACAGG CGTGAGCTAC CAGGCCCAGC 1080
CGGGAATGGG GTATATTTCT ATGTTACTGA GGAATAAAAA TGAGAATACA TAAATATTTG 1140
ACAAATTACC TAGGCTTACA TTACTGGAAA ACTGCAATAT AGCAATAGGG GCCCAAAAAT 1200
ACATTCACAT ACACATTTGC TATACTGTGG AGATATACAC AGCTTTGAGG ACAAGGAATG 1260
GGTAAACATG ACTGTTGCTA CTCCTTATAG CCAGTTCTGC ATAATTATTT ATAAGCATTT 1320
CATAACTTAC TGATTCAGAA GTAAATCAGC ACCACGTATT GTTTTGCACC CAGCAAGCTT 1380
AGCTATTCTG TATCCATCCT TGAGAAAGTA GTCTGATGAC TCTAAGATAT GTCTCTGCTG 1440
CTGATGAGCA GTTCAAAGCT TTCCCTTTAA GGGAGAACAT GTGTTGACTT ACAGAAGAAC 1500
CCCGCTTGCT CCAACATAAC TGCAGAGGTC TGTCTCAAAT CCCTCCTATT CATGATCTCC 1560
CCTGATATAC TCTCTCTTTC TCCTAACGTG TGTTAGAGAG AGACAGAGAG ACAGACAGAT 1620
GGAGACAGAT AGAGGAAACA GAGAGACAGA CACAGAGAAT AAAGCTCTGC TAATCCAGCT 1680
ATTTGAATGA GCGAGCCACG TAAACACAAT CCTTTAGCCA TGGACATGGT TAAGCTAAAA 1740
ATCAAACCAA AGATCCATGA CCACCACTAA GAAGGGCTAT ATATTCAGGT GCAGCAAAGA 1800
GCCAAAGTCA CACACACACA CACAGAAATA CACAAGGCTG CTGGTCACTT ATTGCACCCT 1860
GAGATGTGCT CTTCTGAAGG CTTGTCTAAG TCACCACTTA GACTCTGTAT CTGGATCAGG 1920
TCAGTAAAGA AAGATGGAAT ATTGCTGGTT ATCTTTTATG ACTTGAACTG TTCAACTGCA 1980
ATTCCCTGTC CTCCTGCCAG TCCTAAGAGA TGGCTGGGCT AGTTTTACAG AATTGTTCTC 2040
TGCAAAACAA CATTGGCTTG CTTTTTACAT TGAGTTTGTA AATAGGTCTT AAATTTAGGC 2100
ATTGAGCCAT AATTTCCAGC AGTATAACAT TTCCCTTTTA TGGTTCTTGG AAAACTGGAT 2160
TGTAAAAAAA TGTTACAATA GTTTCCTACT CTGATGCCAA TAAAGATGTG GGTTACTGGC 2220
AAGAAAGAAA GAAAGAACTG ATTTAGTGGG GATGTGGGAG TGTAACACAC ACACACACAC 2280
ACACACACAC ACATATATAT ACATACACAA AATACATACA CACATAGACA CATATGAATA 2340
CTTCTGGCCA GAAAAGACTC CTTTAAAAAT AAAAATCTAC AAATCAATAA 2390
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