| Tag | Content |
|---|
EnhancerAtlas ID | HS127-08050 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr12:111607310-111609990 |
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 | CAATCGGATC AGGGACATTC TTCCACCCTC AGCGGGTCGG CCTGGCTGCC TAACCAGCCC 60
TGAGGATGGA GGGCTGGCTC TCTCCCTGAC TTTGTTCTTT TAAAGAGGAA AAAGCCTCCT 120
CAGTGGCAGG GTGGTTGGCA TATGGGCTCC GCAGCCTGCT TCGCGTCACG TTAATATGTG 180
ATTAAAGGGG TCTTAAAACG CCCATTAGTC CCCCTCTGGT ATCTAATAGC GCTTTTGGAT 240
TTAGAACAGA ATATTATTTA CTCATTAGCT GATAATAGAC CCTGAGTACA CGCCTTATGT 300
ATTGGGACAA TTATTAGAGT CGATTACACA CAGAGACGTG GTTCTGCTGG GGTGGCTGGT 360
GGCAGGCCAG GGTGGTCCAG AGGGCATGAG GGTGGCAGGG AATGACTATG GGCCATATGT 420
GGACAGCAGG GAGCCCGCTA GAGATTGTGT GTGGCAGCTG TGGATGGAAG CAAATTCCCT 480
GTGCAAACAG GGCCACTGGA TGCCCCATGC AAGGTACTAG GGGGAAGAAT TTAAGGAAAC 540
TGCCTCCAAG AATTGGGGTG CCAACAGTAA CAGCCCCTAT GCAGCAGTAA GGGATTGCAC 600
TTGAGCATTC GTCCTGAGTC TCCCAGGATG AGAGTATTAA GAACAATAAC TGGCCAGGCG 660
TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCAG ATCACCTGAG GTCGGGAGTT 720
CAAGACCAGC CTGACCAATA TGGAGAAACC CCTTCTCTAC TAAAAATGCA AAATTAGCCG 780
GGAGTGGTGG CACATGCCTG TAATCCCAGC TACTCGGGAA GTTGAGGCAG GAGAATCACT 840
TGAACCTGGG AGGCAGAGGT TGTGGTAAGC CAAGATCATG CCATTGCACT CCAGCCTGGG 900
CAACAAGAGC AAAGCTCCGT CTCAAAGAAA GAAAGAAAAA AAAAAAAACT GCCCCCACCG 960
TGGATCACAG GATAGGGTGA TGTGCCCAGG ATACACAGCT AGGAAGTGAC TGAAGCTGGA 1020
TGCACACCCC CAGCTCTTCT TTTTTTTTTT TTTTTTTTTT TTTTTGAGAC GGTGTGTCAC 1080
TCTGTCACCC AGGCTGGAAT GCAGTGGCAC GATCTCAGCT CACTGCAACC CCTGCCTCCT 1140
GAAACCCAGT TCTTCTGATG ACAAAGCCTG GGTTCTTTTC AACATCCTCT CCACTTGCTG 1200
CAGAAACTGC TCAATGATTC CAGTCTTCCC CATTCTCCGA CAGAAAGAGG AACTTTGACA 1260
TCACTTCCTC TTATGTGTGG TGTGTTGGAA AGATGAAAAT AGCAGGTTGT TCCTCTCCGT 1320
GGCTGGGTCC CTGACCTCGG GCCCAGCGTG GTAGGAAGGC CGAGGTGGAG GGAATAAGCA 1380
TGTGGAAGCC ATGGGAGTGT CTCCTGGGAA GCGGGAGAGA TTAAGGAGGG ATGGACCGGG 1440
CCCATGTCTG GCATCGGCAA TTCTGGTCAA GGTGCATGGG AATGGGAGGG GAGTGGGGAA 1500
GCGCCAGGTA GGGTCCAGCA AGGTGTTCTG GTTGCCCTGG TGATGCCTCT TGGGCTGTGA 1560
CCCAGAGTGG CGTTGGCATC CAAGGAGAGA ATAGGTGCTG GTAACACCTG GAGTCATCCC 1620
AGCAGGTGTC AGTGGCTGAT TCCACTTGGG GGTGACAGAG ATGGAGAAGT TGGGCAACCC 1680
CCAGTCTGAT GGACGGGGTG CAGAGTATGG AAGGAAAGCC TCGAGTTTGA CCTTCACACA 1740
CACCTTGACC TTGTTGGCAA GCCCGATCTG CAGGTCATCA GTTTGCAGTG ATTTTGCCAG 1800
TGAACACCTG AGCCCCTTAG TGCATTGTGC AGCCTGCTGA GAGCACCAAA AACCTCCCCT 1860
TAATACCCAG ACTCACTGCG GCTTTTCTGA GACCGGCCAG AAGGACAGAC GAGAGGGGTT 1920
TCTTATGCAC CAGTGGGAGT GGGTCTCTCT CTGACCCAAT GCAAGCAGCC CGGAGACATC 1980
TTGCTTCCTT GTTTCCATGG CTTGTGGGGA AACCCCGGTC CCGTGTCCCT GTGCACGCAG 2040
ATGGCTAGTG GCTCAGTGGG TCTCCGGAGC ACAGCCACCT GACACATCTG GGGCTATGGG 2100
ACGGAAAAGC CCAGAGTGCC CTCTCTGAGG AGTCATCCCA GCCTGTGGCC ACAGTGATGC 2160
TGAAGGGGTT TGCAGGCCAT AATTAGGGGC TCAGTGTCAC CTTTGTCCAG TGCCTGAGCT 2220
GAGAACAGGG CTCCCTGGTG AAAGAATGGC AGGGTCCCTT TTCGCCTCCC GGGGAAGGAG 2280
CCGGAGAGAA GGCAGAGCTT GGGAAATTGG CCCTCTGTCT TCTCCCATCC AGATATGTGG 2340
GTCCTGGGCC TTACCTGTAC CAAATAAATA ACCCATTTCC CAATGGGCAG GCAGCATATG 2400
CACTCTCTGT GTGTGCGTGT GCCTGTGCCT GTGTACACGT GCGTGTGTGT GCGTGCATGT 2460
GCATGCACCT GTGTGTGTGT GCATGTGCCT GTGTGTGCGC ATGTGTGTGC ATATGCCTGT 2520
GTGTACCTGT GCCTGCGTAT ACATGTGCAT GTGCACACGT GTGTGCATGC ACCTGTGCGT 2580
ATGCATGTCT CTGCGTGTGC ATATGCTTGT GTGTGTGTGT GCATGTGCCT TTGTGTGTGC 2640
ATGTGCCTCT GTGTGTGTGT TTGTGTGTGT ATGTGCATGT 2680
|
