Tag | Content |
---|
EnhancerAtlas ID | HS092-13592 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr12:120619740-120621370 |
Target genes | Number: 22 | Name | Ensembl ID |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIA | MA0670.1 | chr12:120621286-120621296 | ACTTGGCACC | - | 6.02 | Nr5a2 | MA0505.1 | chr12:120620532-120620547 | GAGCTCAAGGCCAGC | + | 7.45 | PBX1 | MA0070.1 | chr12:120620132-120620144 | TCATCAATCAAT | + | 6.44 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I120181 | chr12 | 120619381 | 120621428 |
|
Enhancer Sequence | GGAGTTTGAG ACTAGCCTGG CCAACATGGT GAAACCCCAT CTCTACTAAA AATACAAAAA 60 TTAGCCAGGT GTGGTGGCAT GCACATATAG TCCCAGTTAT ACTCAGGAAG CTGAGGGTTG 120 AGAATTGCTT GAGCCTGGGA GGCAGAGGTT GCAGTGAGCC GAGATTGCGC CACTGCATTC 180 CAACCTGAGT GACAGAATTA CACTCTGTCT CTCAAAGAAA ACAAAAAAAA AAAAACAAAA 240 AAAACCACTC AGTGCAGATA AGCCAATGAG CTTGCCCCTT CTTACAAGGA GGCTTTTGGT 300 AACAATGACA CCCATTCCCT GAAGCAAATC CAAGAGAGTC CCAGCTCACA ATACGTAATC 360 CTTGACCCTC AAGGTTTCAG CATTCTAATC CATCATCAAT CAATTATACT GACAGCCATT 420 CCATGTTTGT CCCCAGAGGT GCGCTGGATA AGCTCCCAGG GATGCAGCCC TCTATCTAAC 480 CAGCAGGCTG CTTCATGGAG CGGTACTTGT GTTTCCTAAG GCCGGTCATC ACTGGCACCT 540 ACCTGCCTGG GACTCTCCAG TTTCCACAGT CATCTCAACC CTCAACGAAA CCTGGCTTTG 600 CGACAACTCT TTGAGGTGGA CAGGGTGAGT AGTATTTTCT TTCCCACTTT GCAAATGAGG 660 AAATGGGCTC AGAAGTTAAG TGACTCAGCC AAGTCTCATG GACAAGAATC AGATCCAAGG 720 CCTGGCAAAG TGGCTCACAC CTATAATCCC AACACTTTGG GAGGCCAAGG CAGGCGGATC 780 ATCTGAGGTC AGGAGCTCAA GGCCAGCCTG GCCACCATGG AAAAACCCTG TCTCCACTAA 840 AAATACAAAA GAATTAGCCA GGTGTGGTGG CAGGCACCTG TAATCCCAGC CACTCGGGAG 900 GCTGAGGCAA GAGAAACGCT TGAACCCAGG AGGCAGAGGT TGCAGTGAGC CAACACCACT 960 GCACTCCAGC CTGAGCAACA GAGCAAGACT CCGTCTCAAA AAAAAAAAAA AAAAACTACT 1020 CCTCATGACC TACACTAAAA AACCACTCCT CATGACCTAC ACTAAGCCTA CCCAGGCACA 1080 TGTCTGCTCT GCTCACCTCC CAACCTGGTG AGCAGACATG GGGAAAGAAA AAGAAGAGAA 1140 TATGGAAGGA GCAGGTAGAG AATGGAAAGA GGGAATTTAA GAACCAAAAC CAAGACAAAA 1200 AATCCATTCC ATTCACCAGT TCAACACTGA AATCAAACAC AGGGAATGGA ATGATCAGCC 1260 AGAAAAACAC CAAGAGGATT TACACTATGA TATTTTCTAG TCTACTTGAT TTTTGGCTGT 1320 CTTCCCAACT CTGGCCTGTC ACGGCTTCCA CACATGCCAT GAAATCAGGG GCCTCATTTC 1380 TGTTGTGCAT CACTGCATTT CTAGTGCCTA GCACCATGCC TGACAGAGAA GCTCCAAAAT 1440 GTCTAATACA CCAAACAATG TGATTATGCT GCACTCATGG CCATCCACCA AAGCCACACA 1500 CCTCGGGACA ACTCAGAGTG TCTGGTCACC CAGCACCCAG AAAAGCACTT GGCACCAAGA 1560 AGGTGCTGAA ACATGCTCTA ACTCCTGGCA GAAAGCTGAC CCTTGCTACT TCAGAGACAC 1620 AGGGAACCTA 1630
|