Tag | Content |
---|
EnhancerAtlas ID | HS044-06590 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr19:35949520-35950880 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr19:35950051-35950065 | CACTTCCCCTTTCT | - | 6.22 | SPIB | MA0081.2 | chr19:35950051-35950063 | CACTTCCCCTTT | - | 6.07 | Stat6 | MA0520.1 | chr19:35950084-35950099 | CCCTTCCTCAGAACT | + | 6.3 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_10065 | chr19:35949397-35950794 | CD14 | SE_60149 | chr19:35925812-35960098 | Ly4 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH19I035457 | chr19 | 35948818 | 35951260 |
|
Enhancer Sequence | GGGGGAAGGG TAGGAAGCCC TGATCTATTG CATTTGCAAA TTTCTGTGGC ACATACACTC 60 CCACCAGGAA TCATTGCTAC CAATATGAAG ATCTTGAACA TGGGTTTGGC AAGAGATGCT 120 AATAATGGGC TCTTATTATA ATGTAATGAG CTCAGACATA TCCCTGCATG CAACTCACAG 180 TACATCTGCT CAAATGGCAG CCAGATCACA TCTTCCTTGA GAAAACTTTC TCTTTCCCCA 240 CCAACGCTTC ATGCAAGCCT CTTGCACAGT GCTTCCTATA CAGTAAACAC TAGTTAAATG 300 TGGCTGGCTG GGCCTGCTCC AAAGCATCCG GGTGGCTGTA TGATTGCACA GCTCCTCTGA 360 ACCCCCTGCC CCAAAGCAGG ATGACAGATG GGTAAACAGA AATATTAGTG CCTGGTTAAT 420 GAATAACACA GACGGCAGCC TAGTGCCGCT ACCAGGAAAC AGGGGTGGAG GGATCTGACC 480 TGGCCCAACC TGGGGGCCTG AGCAGCACGA AAAGGGAACC TGGCATTATT TCACTTCCCC 540 TTTCTGGAAA AGATGCTCCT GGGCCCCTTC CTCAGAACTT CTCATCAGTC CGCACAACCA 600 GAGCTCAGGT GCAGTGTGGC TTGGTGATGA ATACTATGGT TGGAAAAGGA GGGATGGGGG 660 CAGTGGGCAT GGAGAGGGTC TGGAGGAAAC ACACAGCCAT GATTCCAGCC TCACTCCCTT 720 AAACGTCCTG CCTCTCAGCG CGGGGTCTGT GCTAGTTCTT CTTTTCGCCT TGCCCTGCCT 780 CCTGTGGATA AGTGCTTTTG CCCCACTTTT TTTTTTCCTT TTCATTATTT ATCTCTAATC 840 ACAGGAAATG AGGACATTTC TCATCTACAA ATTGCACATC CCATCAGGAA ATTGGGCCAA 900 AGATCTCTAA GCCTTCAGAA GCGGTCATCC AGTAACCCAC TTGGCAAAGT TTCAAAGGTC 960 TGGGAAAGTA GATGCGAGGT CAAGCAGTGC GGGAGGGGAG CCAACTCTGC AAACGCTGGC 1020 CACGGCCAGC TGGCCACCAG CAGCTTACCC GAGGAGGGGT TGTCCAAGCT ACATACTAAC 1080 CCCGGTTCCC TCTCCCCAAA CATTGTCCTC TGCCATCTGT CAGTCCGAGC TACGACCAGC 1140 CTCGAGAAAA CAGAGTTAGG AAAGTAAACA CACTGCTCCC AAATCTAGCT ATTTTAAATA 1200 AAAAGCTCAC CCATGTGGGC TGCAGTTGAG AATTTCTAAA GTGCCATGGC AAACATTACA 1260 CCATTTGAGT TTCCACGGCG TAGCCTTCAT TCATCCGCCA ACATTTATGG AGGCCTACCA 1320 TGTGTCAGGC CCTGTTTTAG GTGCTAAGGA TACAGCAGTG 1360
|