| Tag | Content |
|---|
EnhancerAtlas ID | HS136-05071 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr12:111607350-111609920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:111609288-111609306 | TCTTGCTTCCTTGTTTCC | - | 6.08 | | GFI1 | MA0038.2 | chr12:111609093-111609105 | TGCAGTGATTTT | - | 6.11 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I111170 | chr12 | 111607961 | 111609004 |
|
Enhancer Sequence | CCTGGCTGCC TAACCAGCCC TGAGGATGGA GGGCTGGCTC TCTCCCTGAC TTTGTTCTTT 60
TAAAGAGGAA AAAGCCTCCT CAGTGGCAGG GTGGTTGGCA TATGGGCTCC GCAGCCTGCT 120
TCGCGTCACG TTAATATGTG ATTAAAGGGG TCTTAAAACG CCCATTAGTC CCCCTCTGGT 180
ATCTAATAGC GCTTTTGGAT TTAGAACAGA ATATTATTTA CTCATTAGCT GATAATAGAC 240
CCTGAGTACA CGCCTTATGT ATTGGGACAA TTATTAGAGT CGATTACACA CAGAGACGTG 300
GTTCTGCTGG GGTGGCTGGT GGCAGGCCAG GGTGGTCCAG AGGGCATGAG GGTGGCAGGG 360
AATGACTATG GGCCATATGT GGACAGCAGG GAGCCCGCTA GAGATTGTGT GTGGCAGCTG 420
TGGATGGAAG CAAATTCCCT GTGCAAACAG GGCCACTGGA TGCCCCATGC AAGGTACTAG 480
GGGGAAGAAT TTAAGGAAAC TGCCTCCAAG AATTGGGGTG CCAACAGTAA CAGCCCCTAT 540
GCAGCAGTAA GGGATTGCAC TTGAGCATTC GTCCTGAGTC TCCCAGGATG AGAGTATTAA 600
GAACAATAAC TGGCCAGGCG TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCAG 660
ATCACCTGAG GTCGGGAGTT CAAGACCAGC CTGACCAATA TGGAGAAACC CCTTCTCTAC 720
TAAAAATGCA AAATTAGCCG GGAGTGGTGG CACATGCCTG TAATCCCAGC TACTCGGGAA 780
GTTGAGGCAG GAGAATCACT TGAACCTGGG AGGCAGAGGT TGTGGTAAGC CAAGATCATG 840
CCATTGCACT CCAGCCTGGG CAACAAGAGC AAAGCTCCGT CTCAAAGAAA GAAAGAAAAA 900
AAAAAAAACT GCCCCCACCG TGGATCACAG GATAGGGTGA TGTGCCCAGG ATACACAGCT 960
AGGAAGTGAC TGAAGCTGGA TGCACACCCC CAGCTCTTCT TTTTTTTTTT TTTTTTTTTT 1020
TTTTTGAGAC GGTGTGTCAC TCTGTCACCC AGGCTGGAAT GCAGTGGCAC GATCTCAGCT 1080
CACTGCAACC CCTGCCTCCT GAAACCCAGT TCTTCTGATG ACAAAGCCTG GGTTCTTTTC 1140
AACATCCTCT CCACTTGCTG CAGAAACTGC TCAATGATTC CAGTCTTCCC CATTCTCCGA 1200
CAGAAAGAGG AACTTTGACA TCACTTCCTC TTATGTGTGG TGTGTTGGAA AGATGAAAAT 1260
AGCAGGTTGT TCCTCTCCGT GGCTGGGTCC CTGACCTCGG GCCCAGCGTG GTAGGAAGGC 1320
CGAGGTGGAG GGAATAAGCA TGTGGAAGCC ATGGGAGTGT CTCCTGGGAA GCGGGAGAGA 1380
TTAAGGAGGG ATGGACCGGG CCCATGTCTG GCATCGGCAA TTCTGGTCAA GGTGCATGGG 1440
AATGGGAGGG GAGTGGGGAA GCGCCAGGTA GGGTCCAGCA AGGTGTTCTG GTTGCCCTGG 1500
TGATGCCTCT TGGGCTGTGA CCCAGAGTGG CGTTGGCATC CAAGGAGAGA ATAGGTGCTG 1560
GTAACACCTG GAGTCATCCC AGCAGGTGTC AGTGGCTGAT TCCACTTGGG GGTGACAGAG 1620
ATGGAGAAGT TGGGCAACCC CCAGTCTGAT GGACGGGGTG CAGAGTATGG AAGGAAAGCC 1680
TCGAGTTTGA CCTTCACACA CACCTTGACC TTGTTGGCAA GCCCGATCTG CAGGTCATCA 1740
GTTTGCAGTG ATTTTGCCAG TGAACACCTG AGCCCCTTAG TGCATTGTGC AGCCTGCTGA 1800
GAGCACCAAA AACCTCCCCT TAATACCCAG ACTCACTGCG GCTTTTCTGA GACCGGCCAG 1860
AAGGACAGAC GAGAGGGGTT TCTTATGCAC CAGTGGGAGT GGGTCTCTCT CTGACCCAAT 1920
GCAAGCAGCC CGGAGACATC TTGCTTCCTT GTTTCCATGG CTTGTGGGGA AACCCCGGTC 1980
CCGTGTCCCT GTGCACGCAG ATGGCTAGTG GCTCAGTGGG TCTCCGGAGC ACAGCCACCT 2040
GACACATCTG GGGCTATGGG ACGGAAAAGC CCAGAGTGCC CTCTCTGAGG AGTCATCCCA 2100
GCCTGTGGCC ACAGTGATGC TGAAGGGGTT TGCAGGCCAT AATTAGGGGC TCAGTGTCAC 2160
CTTTGTCCAG TGCCTGAGCT GAGAACAGGG CTCCCTGGTG AAAGAATGGC AGGGTCCCTT 2220
TTCGCCTCCC GGGGAAGGAG CCGGAGAGAA GGCAGAGCTT GGGAAATTGG CCCTCTGTCT 2280
TCTCCCATCC AGATATGTGG GTCCTGGGCC TTACCTGTAC CAAATAAATA ACCCATTTCC 2340
CAATGGGCAG GCAGCATATG CACTCTCTGT GTGTGCGTGT GCCTGTGCCT GTGTACACGT 2400
GCGTGTGTGT GCGTGCATGT GCATGCACCT GTGTGTGTGT GCATGTGCCT GTGTGTGCGC 2460
ATGTGTGTGC ATATGCCTGT GTGTACCTGT GCCTGCGTAT ACATGTGCAT GTGCACACGT 2520
GTGTGCATGC ACCTGTGCGT ATGCATGTCT CTGCGTGTGC ATATGCTTGT 2570
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