| Tag | Content |
|---|
EnhancerAtlas ID | HS092-10993 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:132501510-132504160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr11:132503612-132503632 | TGTATGGGTGTGGGGTGGGG | - | 6.18 | | TFAP2A | MA0003.3 | chr11:132502109-132502120 | TGCCTCAGGCA | + | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I132631 | chr11 | 132501679 | 132504056 |
|
Enhancer Sequence | CGCCCGGCTA ATTTTTTTTT TTTATTTTTA GTAGAGACAT ATATTTTTAA ACCACGACAA 60
GAAACCTAAA AACTAGTTTA ACAAGAAAAA TATATTCACA TTTAACTCTG TTTACGTTTT 120
TGAAAACTTA CCCTATGATC AAAATATTAT TAAAAAGTCA ATAGATTAAC AATATTAGGA 180
AATAGATTTA AAAGCACAAG ACAGGTAGTG TCTACAAAAT CCTTCAGCAT GGCAAGACGT 240
ATCATGGAGT ATTTATTAAG ATCACAAGTC AAATCAATAA ATTCTTTGTG TGTGTGAATG 300
TGTGTTAACA TCCAGGACAT CTGTGAGACC CTAAGGACCT ATTCACAGAA GGCCACTGAA 360
TTATAAGTTT TGTCCAGGTT TTCAGCTGGG TAACGAAACA CGTAGCTGGA AATGAAAATG 420
TGGCAGCCAT GCTGATCAGG GCTGGGCTGT TAAAATGGTT TCTGCCTGAA AGAGTCCCTC 480
CTGTAAACAT CCCTAGGATA GGGAATGCAG ATCCAGCTTA AAAAAAAAAA AAAAGAAAGA 540
ATGAGAACAT GATTGTGCCA CATGGAGATT TGGGCAGGAT CTTGTTAGGC CCCTGAGGGT 600
GCCTCAGGCA TCTTTATTCA AACACATTTT TTTTTTTTTT TTTTTTTTTT GGAGGGAGCA 660
AGGAGGAGAT CACACAGTTG TGGAACTGTC GTCAAAGCAA GCAGCTGACA TTTAAATAAT 720
ATTATGATTT AAAAGGTTCC TTTGCATTCG TTCCTTAACT CATTACACCT TCACAACTCT 780
GTGACACGAG AAGAGGAGGT GACACTATTT CCATGTGAAA AATGAGAACA CTGATATTCA 840
GAAAGATGAA CTGATTTTTG TAAGGTCAGA TATCTTTTAA GTAATGGAGC AGGGACTTCA 900
AGTGATGTCT GTCTCTCTCC AGTGGCTCTA TGATTCTCAG GATATCATCC TATCTCCACG 960
CAACACAATG TCGCCGCAGA GGAGTCGCTT CCTGAGTGGT TCCATGATAG CCAGCCCGGT 1020
ATATCTACTC CTTTTGGTCT TTTTCTGCTT CCCTATCTTC AGCAAGGCGA GGTAATCACT 1080
CTCTCTTTGG TATGTGAGAT ATGTATCTAT TCTGTCATAT CCGCCTTTCA GTTGTCACAT 1140
AGCCAAACTA TGCAAATGTG GCCATCTCCA CATCTCTGCG TTCAGCACGG CTGCTGCTCC 1200
ACTCTGGACT CCTTCCAACT GTTCAGATGG GCAGGGAGGA GTTTCATCAT CAGAGATGAT 1260
AAAGAAACAT GACTATTCAG CCTTTCTCGT ACATCTACCG AATACCTAAC TAATGATGTT 1320
CTCACCATAT TGAAAAAAAA AAAAAAAACC ATCCAGGATG ACGAATTTAT TCCCTGAGTG 1380
CCTCATGACA AGTGAGTCAG CTCTCAGCAA CCAGAATTAC AAGTGGACTG AGCTGGGTGA 1440
CGGTGGAGCA TGAGGAAGTG CAGTCTGTCC TGCCTATAAA GGTGGTCCTA GGCTAATCGA 1500
AAATCTGCAC CAACAACACA GCAAAGTGTC TTCTGCTGCC AGTAACAGAG CACCCAACTG 1560
TTGGTGTTTG AGGGGGACAA TCGGTAGCTC TCTCTCTTTT TTTCTGAGAC AGAGTCTCGC 1620
TCTGTCGCCC AAGCTGGAGT TCAGTGGTGT GATCTCGGCT CACTGCAACC TCTACCTCCT 1680
GGGTTCAAGT GATTCTCCTG CCTCAGCCTC CCGAGTAGCT GGGACTACAG GTGCTGGTAG 1740
CTCTCTTTTC CCTGCCTAAG TTCAGAACAA CTTGAGAGAC AAACAGGGAG AAAATAGATG 1800
GAAATAAAAA TAGCCCTTCA TTTCTGATAG AAATTAAAAG CCGGGAATGT GGTTTATATC 1860
TTTACGTAAG CAAATGGGCA TCCCAATCCT GAGCCTCAGG ATTCGACCCC ACTCCCCCAG 1920
TCACAGGAAG TGCGAGGAGG CCCCAGGCCC TGGGTCTGAG CCTGGCCTCT TACGCTGCAT 1980
GACACAGGAC ATCTGTTGGA AGGTCAGTTT CTAAGACAAA ATAAAGAGCT GATACCTCCT 2040
GATTTATCCT TCCACAAACC TGATCAGATT GAGCCATCTC TTCTCCCTGG TGGTAAGGGG 2100
TGTGTATGGG TGTGGGGTGG GGACAGCAGG AGGGAAAGTA AGGGAGGGTG CCAGGAAAGG 2160
CACAGAGTGT TACTTGGTAG AGTTTCTTTT GGGTAAAAGA GGCATCAATA ATGTTTCCTT 2220
CCAACACCAA CTAAAAAGGG TTTCAACAAG AAAGACGTTT ATTACCTCAT GTAAGAAATC 2280
GGGGGTGGGA GGCTGGGGGT GGAAGTCAGG GCTACAGTGA GAGCCTCAAG GCCCAGGTTC 2340
TTCCTGTCTT TCTTCTCCAG TGTGTGGCTT GGACCATCAC AGTCAAAAGA TGGGGGTAGC 2400
AGTTGCAGGC AAGCATACAG ACACAGCAGT ATTTAGCAGA AGCAAAAAGG GAAAGGGGAT 2460
TTTTCTTGCA TGTCACCTTT TGTTAAGGAA GGAAAGCTGC TCCAGATAGC TGCCCTCGGA 2520
CTTCCCCCTG GATCCTACTA ATTAAGATTT GATGGCCTGG CTATGCCCAG CCTGGCTTCC 2580
AGGGTGTCTC AGAAAATGAG TTTATGGTAT TCGAGCTTCT TTAGAGGAAA GTGGCTTCTC 2640
TCATAAAGGA 2650
|
