| Tag | Content |
|---|
EnhancerAtlas ID | HS092-12506 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:69393630-69395510 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr12:69393979-69393991 | GTTTGTTTGTTT | + | 6.32 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH12I069001 | chr12 | 69394045 | 69394110 | | GH12I069000 | chr12 | 69394284 | 69395705 |
|
Enhancer Sequence | ATTCTGATTC AGCAGGTCTG AGGTTCAGCC CAAGATTCTG CATTTTTAAT AAGTTCTCAG 60
GTGATGCCCA TGCTGGAGGT TCATGGACCA CACTTTTGAG TAATAAGGGT TTAGTGGATG 120
GTGACTGTTT CCTCTCTTGC ATTTTCTGCA GTTATGAAGA AGGGGAAGAG CAGAGCCTGC 180
AGGTATGAGC TCCCGAATTG ACATTTCCTA TCTTTAGAGT CCAGGAAAAT TGTATTGCAT 240
TTACTTTCTA AATATTTGCT TTTCTGATCC CAAGATTGTT CTTCATGTAC CTGTATAGGC 300
CACACTTTCG GCAATCCGAG GACTCACACA ATGATATTAA AATAAAGTTG TTTGTTTGTT 360
TTGGGTGAAC CATGATTTTA ATATAGCAAA CTCAAAGGAG CCAGAAGACA TGAGGGTTGA 420
CTCACCAGTC ACAATGGTGT TGTCACATTG TTTATCCGTA TGATAAGCCA GACAGCTATT 480
GCAGGAAGCT GTCAGTTCAC CAAGTCCAAG TTTGAGAAGG TTATTTTTCA CTTGATATTT 540
AAAGAAAGCA GAAATAAGAT GCTGGGCCAA AAACTGTGTC AGAAGATGGG CTGGAATAAT 600
TTCTTTCAAG AAGCTCAGTG GCAATACTAT CTTATAGTTG TTTATTGATT TACCATTACA 660
GAGCACCTTC ATCTGAGTTA TATCATTTAA TCTTCATGAA AACCCTAGGA GGTAGCCTTG 720
AAAAAAAAAA AAAAACAGAG AAAGAAACAA GGGCCAAGAG ATAGTGATTT GTTCAAAATC 780
ACTTGCTAGA GTGGATCTGG GACTAGAACA GAAGTCTTCT AGCCTAGTCA TCTTCTTATG 840
ACAACATTGG TAACTATATC ACATGGATGT TTCTGTTATG CCTTCTCAAG AAGGCATCAA 900
TAATTGATCC CAGAAGTGTT TTTCACTCGA GCCCTTAGCT TCACAATCCT CCCAACTCTA 960
TGCCCCAGAA AGCTAAAAAG CCACTGCCAA GGAAATGGAT GTGGTGTGGG ACAAGAAACC 1020
TATTTTCCTC CTGGCAACAC TAACTTTTAT TATCCACAAG GACTAATTAC AAAGAGATCC 1080
ACTTTTCTTG GGTATCTGTA AGAGGATAAG CATTCATTTT TCAGGTTTGG TTAAGGATTA 1140
TTCATGTGGG GGCAGAGAAT GACTCTGGAG GCCCTTGTCA ACCCTGGAAT TCCAGGAAGT 1200
TAACCTTATA GTTTCCCCAT GCCATTGCCC TGATGTTACA GTGAGAGGCT ATACAGGCTG 1260
AGGCAGGCTG AATTCTAAGA TAGGTCCCAG GATTCCTACC CCCTGACGTT CACCCCATGT 1320
AACATCCTCC TCTTGGATTT GATTGAGACT TCTGATCTAC TTCTGATCAA TAGAATATGG 1380
TAAAGGTAAA GGGATTTTTG TAGTTGTAAT CAAGGCCCCA AATCAGTGTG TTTTGAGTTA 1440
ATCAAAAGGG AGATTATCCT GGATGGACCT GGTTTAATCA GGTACAGGAC TCTCTCTTAG 1500
GTCAGACTCT CTGCTGTTGG CTTTGAAGTA CACTGCCATG TTGTGAGAGA AAGGAGAGGA 1560
TCGCCTGGCA AGGAACTTCA AGTGACCTTT GGAGCTGAGA GTAGCCCCTG GCCACAGCCA 1620
GCGAGAAAAG GGACTTCAGT CATATGAACA CAAGGAAATG AGTTCTACCT GTGATCTTTG 1680
GAAGCAGATC TTTCCCAGTT GAGCCCCCCA GATGCAAATG TAGCCTGGCT GACACCTTGC 1740
TTGCAGTCTT GGGAGACCCT AAGCAGAGGG CCCAGTTAAG CCATGTCCGG CTTCTTGACC 1800
CACAGGAACT GTGGAGTAGT AAAAGGGTGT TGTTTTAAGC TGCTAAATTT GTGATAACTT 1860
TTTATGCGGT GATAGAAAAC 1880
|
