| Tag | Content |
|---|
EnhancerAtlas ID | HS141-04785 |
Organism | Homo sapiens |
Tissue/cell | NB4 |
Coordinate | chr12:117041930-117043570 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr12:117042291-117042302 | TTTGTTTACTT | - | 6.62 | | ZNF263 | MA0528.1 | chr12:117042130-117042151 | GGGGGAGGTAGGGGTGGGGAG | + | 6.38 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I116603 | chr12 | 117041023 | 117043405 |
|
Enhancer Sequence | TGTCCAGTTT TTTTTTTTTT CCTTGGTAGC GATCAAAATG TCGCGAGTTT CTACACACAT 60
ATTTTACAGA CGTTCCATAA ATCTTCCCGT GGTGCCTCTT CTCTATAAGT AAGGTCCCTT 120
GGGAAGTCAT TGAGGCTTCC TCACTACATG TATTCAAGAG AAAATTGGTT GTAACACTTA 180
GAGAAGGCGG CTGTCCGGGA GGGGGAGGTA GGGGTGGGGA GTGTGGAGAA GCTAGTCCAA 240
GTTCAGTTGC CAAGGACAGA GAGACAAGGA AGCCTCCTTT TCTTGGAAAT TCCTGAAATT 300
TCCAAACTGT CTTTTACTTC TCATGCACAA ATAATCTCTT TGTGCTATCT TTTTTATCCT 360
TTTTGTTTAC TTATTTCTAA TCGCCAGAGG GGTCATTCTT TCGCACAAAA TCTGAAAAAG 420
TAGACAGAAG TAGAAAGAAA GATACAACCA ACCAAATAAA CAAAAATCCC ACGACAAATT 480
CCAAGGTTTT TTTTTGTTGT TGTTTTTTTT TTTTGCTTTG TTGTATTTTG TTTTGGAAGG 540
ATTTTCCTGG GCAGTTTGAC AGCACCGTTT CAGCGATGGG GGCCCAATGT TAGTGACAGT 600
TCCGCAGGGA GCTTGTTAAC ATTGCAGAGT CCCCCAAGCC TGCACCCTTG AGAGTGGGAG 660
TTTGTAGGTC AGGGGGGTTG GGTCCCCCAA ATCTGTGTTT TTAATAAGCC CTTGGGTGAC 720
TCCGAGGAGG GCGGTCATCG GACCACACTT TGAGAAATAA TGAGTTTCAG ATTTTTCAGA 780
CCCTCAGCAA ACCTGAGATG TGAAAATCCA GATTTAAAAC AAAAATCGGG GGCTAATGAT 840
TTGTTTTCTG GAAGGGCTCG GCTTAAATAG GCATTTCCCT TAGTGCCGTT AACATATGAT 900
TCTGTTCACA CTCGGTGATT CAGCGAGGCA GCCAGGACTT CATCTGCACC ACTCTGGGCC 960
AATACGGCAT ACCGCCACCT TTTTACCGAG CAGCGTTGAC GCCCATCTGC TCAAATAAAT 1020
TAACGTTTCC ATCTCAAATA ACTCATTTGG CTGGATCATT GAGGTTACAC GCCAACCCGA 1080
AGAGGAAGGG GAGGAGGCAA TACAGGGGAG GGGGAGAGGC AGGAAAGGCA TTTTGCAACG 1140
TATAAGTTGC AAGTAATACC GTTGCATTTT TGTAGCCAGA AAGGAGGGGT GAGTAGATGA 1200
ACACAGCTAC TAGTGTAATT CACATGCACC CTTTTATTAT CTGCTTTTCA CGACTCCTAC 1260
TGATGCTTCG GAGGAGGGTA CAGCTTGCAG CTGGATTCGC TGATGGGCGC GATATTCCCT 1320
GTGCAAAGAC ACTGTGGAGT TTGTGTGAGC ACATTGTGTG TGCATGGGCA TGAGTGTGTG 1380
TATGGGGGCG AGGGTAAGGG GTGGAGGATT GTTCTGCAGA AGATCATGAT GTTCAGTGAG 1440
ACGTACAGAG AACACACAGA GGAGACAGCA GGTAGTTTCT TTCCTTTTTT TAAATGGACT 1500
TTATTTTTTA CAACAGTTTT TGACTTTTAT TTTGAGAGTT TCACTGCAAA ATTGAGCAGC 1560
AGGTACAGAG ATTCCCCATA CACTTCCTTC CCGAAACATG TGCTGCCTCC ACCACCATCA 1620
ACATCCTGCC CCAGAGTGGT 1640
|
