| Tag | Content |
|---|
EnhancerAtlas ID | HS055-03480 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr17:54767060-54769300 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr17:54767886-54767903 | TGGTGTCTAGGAATTAA | + | 6.54 | | MEF2C | MA0497.1 | chr17:54768320-54768335 | TTTTATTTTTGGATT | - | 6.33 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I056690 | chr17 | 54768341 | 54768490 |
|
Enhancer Sequence | AAAAAGAAAA GAAAGCCGAG AGGCCAACTA ATCCAACACA CCCCTACCCA CCCATTTCAC 60
AGAGGAGAAA GTTGAGGTCC TAAAGGAGTA AAGGATGTGA GAAAGTCCCA CATCTAGTGA 120
GTGGCCATGT CAGGTCAGCC TTGACCCCTG CCTCTCAACT CCCAGGCTTG TGCTCTTTCC 180
TTTCTAGCAG TAGAGTGCTG AACTTGCTGT TTGCCCATGC ATTTGGGGTT GGGACAGGGG 240
AATGGACATT GAGAAAGGGA TTGCTTTAAT TAACATAGAC ACAGAGGAGG CATGGGCTGG 300
GCAGGTGATG TGGCAGGGGG GAGTTTCAGA AGGGATTTCC AGGTCACTGA CTGTGCCAGG 360
CTCCAAGTTC CAGATGCTTT TTGTCATAGG GGCCCGTCCA CATGACATCC GCCACCGTGG 420
CACAGGCTGG AGGACATGCC CTGCCTGACC AACATTTTAG GGGCTGGAAG ACGAGAGGAA 480
TCTTCCTGGA GAGAGGCTGG ATTCTGTTCC TAGCTGCACT GGGGATTGAC GAGGAAGCTA 540
ACTTGAAAGG TAAGGTGGTA TACCAGAAAG CTCGTCAGAC AAAAATTCAG TTAAGCTTTG 600
GTTCTGCTCC TGTCTTATTG TGTGACCTTG AATCTTTCCC TTAACCTCTC AGAGCCTCAG 660
TTTCCTCAGT TATATTAAGT ATCACAGCAC CTGCTATTCC ACCTACTCAC AATTGTGGGA 720
AAACTCTAAT CTAACCCACT AATTAGATAG ATAAGGAGCT CACAAATCCA TTTGTATACA 780
ATCCTGGACA TGGGTGAGAT AATAATAAAA GGTGGTTTGC ACATCCTGGT GTCTAGGAAT 840
TAAGGTACAT GAAATTACCC AACCACACAC CGCTTCCTGA GTCCAGAGGC TGGAGAGATT 900
TCAGCAGCCT CCATTTCAGG GCCAGTGGGA TTCTTGAAGA CAAAGGGAAA AATGTTCTCA 960
ATTCCTTTGT CGAGAGACTT ACGTCAACAG ATGTCCCAGA TAGAGACACT CAGGATGCGT 1020
AATGGAATAG TGCCCACAAG GAATAGGGGC CCAGGGAGCC CTCAAAGCTC CAAGTCCTGG 1080
TCCTGCACAT GGAGCTCCGG AGAGAGGCCA GGACGGAGGC TGGGATCCAG GGCAGGAACA 1140
TGTGGAGGAG GAAAGGCGAA TTGGCCAGCT CTGGGGAGAC ATCCCAAACA TCCGGAACCC 1200
ATTGCTCAAG CAGGGCACTG GGCTCCAGAG GCATGCTGAG CGGAAGATGG TGGGGTTTTG 1260
TTTTATTTTT GGATTTTGCC AAATCAAAAG AATTCAAGAA ATTGCGGGAA CTGTTGTGTT 1320
GAAATGCAGA CACTGCCAGG GTTGGCACAG GCCTGTTTAT AAGTAATTCA GTCTGAAGCA 1380
GGGAGGAGCT GCAAGCGTGC ACACATGCAC ACTCACACAC ACTCGCACAC ACATACTGCC 1440
TGCACAGGCC AGTGGCCACA GGAGGCCTGA TCTTCCCTTG GTGGCTCCTG AGGGGTTGGC 1500
CAACACACGC GGGCTCCAGG CCAATGTTCA TTCATCTGTG CACTCCTGTA TTCACTGAGT 1560
GCCTACGACG CAGCAGGCAA GTCAGAAGCT CACAGATGGT GTGGGGAGCA GAGGCGGCCC 1620
CTCCCTTCCC AGTACTGACG TTCCTCAGGG CCATACAATG GTAGGGGATG CAGGTCCCCC 1680
CTTTTTATCT GAGCCTAAGT AGAGAAGAGT AGGCGATGGG CTAGGGAAGG AGAGCAAAGG 1740
GTAAGGAGAC ATGTAGCAGA CACTGGTGGC TCCCCACCTA TCACCCATCC ATACTTCCTG 1800
CTTTTGCTCT TGCTCAGGCA GCAGTCAGGG ATCCCTTGAT CTTGGGGAGA GGAGACACCT 1860
TCCCAGTCTT AGGGGATGCA TCATAACAGG TCCAAAATAA TTGTGGTCAC CTCATTACCT 1920
TTGGTTAGTA ATTGGCCTGA AGGTCTACAC ATGTGACCCA GTTTTAGCTA AAAAGCTATA 1980
AGAATTCTCC TGGGAGAGCT AAGCTCTTTT GCCCTTCCCC TTTCTTCTTA CTAGAACATG 2040
GACATAAGGG TCAGAGGTGT CAAATCCATT TGAAAACCAA GAGGCAACAT GTCAACAAGC 2100
TAAGATGGCA GGACTAAGAG AAAGAGCCCG CATGTTTGAC AGCACCGAGC CATTGCACCA 2160
GAGTTGGAAT GCCTGCCTTC AGACATTCAT CAGGTGAGAC CAAATAGAAA TCTATATTTA 2220
TACTATACAT TTATTAAATA 2240
|
