| Tag | Content |
|---|
EnhancerAtlas ID | HS092-13926 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:133299740-133302250 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:133301468-133301487 | ATGCCACCAGATGGCGGCC | + | 6.66 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I132723 | chr12 | 133300461 | 133302372 |
|
Enhancer Sequence | CACCGGCTGC CTGCTCAGAG GACTTCCGCC AGTGGCCTGG GCCCTTTCCA AATCCCTGAC 60
CAGGACGGCA AGGCTGACCA ATGGTTGTGG AGACAACAGC CACAGCAACC ATACACCACT 120
GTCTAGAAAT AGTTTGATAA GCCAGGGACG CGCCAACTTC AAAAACAAAT ACCAGGCACG 180
CTCACGTTTG ACCTCAGACG GGAGCAAGGC TGGCGAGGAA GCAGTCCGGG ATGCTCTAAG 240
TCAGCTACAC AGGGCGCCCA CGCCACAGCC CCAACGCTGG GCCTCCAGGG ATGGGGCAGC 300
GCTGCAGGGC TAAGCCTTTG TTCTGCTTAG GGCCCCGGCT CCTCTGTAAA GTGGGAAAGC 360
TTGGAGGTGG GAGCAGCGCC AGCACGCCTG GCACTGAGGC AATGCTCAGA GCAGGCGCAG 420
GTTTGCTGGG CAGCAAAGCT CATCACAAAG TGGAATGACC ACACATCAGC TGGCCCCAAT 480
GCCCTGCGCA GCCCACGGCC ACTCCCATCG CTCACGTCAT AGACGTGAGT CGCACTCATG 540
TGAAGATCTG GACAGACTAC CTGGTCTAAA GGGGGAAGTG GATGGGAGAC CACGAGCAGT 600
TTTCAATGGA TCACAAGAAA CCAGTGACCC AGAGTCTTCA AATCCTTCTG CAAAAAAACA 660
AACAAAACCC AAAAGGAAAG AAAACCTGAT TATGCTGCTT AAGTCAAATC TGAAGTCAAG 720
GATTTTGAAA AGTTAAGCCA CAAACTCAGT GTGTGACTAA TTCTTTAAGA GCGTACAGCA 780
ATGATAACCA AGTCTACAGC CCTTGGTATT CCCAGGCAGC CTCCACTCCA AGTCCTAACC 840
AGGCCCTGCT TATCTGCCAA GATCAGAGAG ACTGGGTGTG CTCGGGGTAG TATGCCCATA 900
GATGATTACC TAAGTTTCTT GAATATGAAA CTTTAAATAA TTTTTAGTTT CTTTTTCTAG 960
AGTAAATTCC CAGCAAACTT TTTTTTTGAG ACATACTCTG GCTCTGTCAC CTGGGTTGGA 1020
GTGCGGTGCC ACAGTCTCGG CTCACTACAA CCTCCGCTTT CCAGGCTCAA GCGATTCTCA 1080
TGTCTCAGCC TCCCAAGTGG CTCGTTCTAC AGGTGTGCGT CACTGCACCT GGCTCATTTT 1140
TGCATTTGTG GTAGAGATGG GTTTCACTAT GCTGGCTAGA CTGGTCTCGA GCTCCTGGCC 1200
TCAAGTGATC CGCCCACCTC GGCATCCCAA AGCACATGAG CCACTGTGCC TGGTAGACTT 1260
CCCTTCTAAA ATACCTGCTG TTCAAAGTGG TTCTTCCTTA AATGGCCTTT TCCAGTCTTC 1320
TGCATGTGGG ACGGACGTAG ATTAGCAAAG TGAGGATGGC TCCCGGTTTG GCTGGTAGCT 1380
GGTGGGGGTC TAATTTCTGA ATGCTGGACT CAGGGCAGGT ATGGCGGGGG AGAAGGCAGG 1440
GAGGGGCAGG CAGGAGACTG GGGAGTGGGG AGCTGACCCA TACCAGGGCA GCCCCCAGGG 1500
ATCTTCAGTG TGCATGTTGT GAACGCCTGC GTGGAGGGAG CCGCATGAGG GGAAGGCTGA 1560
GGGTGTCTGG ACTGGGTGAG TTACAGGGGC CCAGCGACGT CAACGATGGA AACCGTCCCC 1620
TGGTTTGGGA CAGACTGAAG ACTTCTCACA TGTTAGTAAC GATAGCCTCT GTCTGGCCAA 1680
AGTGAAAACT GCACACCAGA AGCCTCAATG AGACTGGTGG GAAAGGCAAT GCCACCAGAT 1740
GGCGGCCAGC TGCCAGGGGT CGCCATGCCG ACGTTTATCC CAAAGCCTTT TCTAAGGAGG 1800
GAGCACGGGC GGGAATCTGC AGCTGGAGCA GTCACAGGGT TTCCAACCAC GACAAACACG 1860
CCTGCACCCC GCACGCACAG CCGGGCCCCA ATGAGGGTTT CCATCAGCCC TTCCCTGGGA 1920
AAACTCTGCA GGCTTCTGGA AACATCCACA CGGCTCTGGA GGACCTGGCT GTGGTCCCTG 1980
CCATGGCGCC GCTGGCACTC CCACGGCTGG TACGCAGCAC CATGGCTGCT TTTACCCAGA 2040
AACGAGCAGC AGACTCACCG GGCGCCTCCC TCACAGCTGC CACCACGCTG GAGAAGGGCA 2100
CTTTCCAACC AAAGCCACCA CAGCAACTGT TAATGTCACC AAGGTTTCCC ACTGCCAAGA 2160
GCAACGGTAA AATCTGTGCT CTTTTAACGG ATGCCAGAAA ATCTTTCACA ACTGAGTCAA 2220
GAAAGGGGCT TAAAAACAGC GAGCGAATCT GAGGGCACCC AGGTTGATGG CCGTCCAACC 2280
AAAACAGTGC CGTGCGCCTG GGCACAAGTG AGGGATCCTT CCGAAAGCTT GCAATTATTA 2340
CCACGCGGTT TTGAAGTAAT TCATTTCATT AAGTGTTTTG TGAAGGACAT AACCCCCCGG 2400
GACACACGAG AATGCCTCCG TTGGGACTGG AATCGCTGCC CACAAACAAA CGGAGAAACA 2460
GTCAAAGGTG GCCTAAGACC TGGGAAATCA GGAGCAGTGG TCCACATACA 2510
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