| Tag | Content |
|---|
EnhancerAtlas ID | HS060-08862 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr12:122364890-122365800 |
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 | chr12:122365502-122365516 | CACTTCCTCTTTTT | - | 7.38 | | SPI1 | MA0080.4 | chr12:122365194-122365208 | TACTTCCTCTTTTT | - | 7.95 | | SPIC | MA0687.1 | chr12:122365502-122365516 | CACTTCCTCTTTTT | - | 6.4 | | SPIC | MA0687.1 | chr12:122365194-122365208 | TACTTCCTCTTTTT | - | 8.42 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I121927 | chr12 | 122364907 | 122365905 |
|
Enhancer Sequence | AAAATTCAGA CAACTTATAC ATGTTTGAAG GCAAAGATTC TTCTTCCTAC ACACACCCCC 60
ACCCAATCTC ATTTCCCTAT GTAATTCCTG CCACAGTTGG CTGTGACTGC TCCTCTCCTG 120
ACCTTGTTCT GTGCATGTAC AACATGTTAT CTGTGTGCCC ATGCCTGTGC ACATGGCTCA 180
CATTTAGTTT TTGTGTTGTT TAGGTTTTTT TTTTTTTTTA CCGGTGAGAT AATCCTGCAT 240
TTCTACAAAA TGTTTTTCCA CTTAATATGT CTTGGAAGGT TTCTTGTATC AGTGCATGTA 300
TCTCTACTTC CTCTTTTTGT TTTTCTTTTT TTGAGATGGA GTCTCACTCT CACCCAGGCT 360
GGAGTGCAGT GGTGCTATCT TGGCTCTCTG CAACCTCTGC CTCCCTGGGT TCAAGTGATT 420
CTCCTGCCTC AGCCTCTCAT GTAGCTGGGA TTATAGGCAC GCACCACCAT ACCCAGCTAA 480
CTTTTGTATT TTTGTAGACA CAGGGTTTCG CCATGTAGGC CAGGCTGGTC TCGAGCTCCT 540
GACCTCAGGT GATCCACCCA CCTCAGCCTC CCAAAGTGTT GGAATTTCAG GCATGAGCCA 600
CCGTGCCCAG CCCACTTCCT CTTTTTAAAT GTAACTGTTC CCCTTTCTGT GGCCATTTAG 660
GTTGCTTCTA ATTTCTTGCT GTCACACAAG GTCCTACAGT GAACGTGCTC CTCCATCTCT 720
CCTGTGTCCA CAGCATCCTC CTTTTCCTTT GGGGTCCTCT CCTTAGTGCT AAGGCCTGTA 780
CTAGCTCCCA TTGTTCACGG TAAATAGACA TGACTGTGGA TCCCACCTCC AGCTAGGAAA 840
CAAGGCAATC ATGTATTTAT GAGCAGGAAT CTTATGAATA TCAAATACAA TGAAATCTGG 900
TTTTGACAGC 910
|
