| Tag | Content |
|---|
EnhancerAtlas ID | HS044-13634 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr9:119233140-119234770 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr9:119233641-119233652 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr9:119233641-119233652 | TTTCCCAGAAA | - | 6.32 | | ZNF263 | MA0528.1 | chr9:119233880-119233901 | GGGGGTGGAGGGAGGGGGGAA | + | 6.59 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_40330 | chr9:119232727-119234862 | K562 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I116470 | chr9 | 119232534 | 119234863 |
|
Enhancer Sequence | TTATGGTGGG TACTCTCCTT GGCCTGCCAT TGGTTACCTA CATTGGGACA AGGGTATTGA 60
GATTCCTGGA AGAAAGTTAT AACTCTAAGA CGATGTATTG TTCAAAAATT AACAAGACTA 120
AAGCAAAAAC AAACAAATGA AAAATCTCTG GGGTTTCCTC TCCTTTTTCT TTTTTAAAAT 180
GATTTTTTAA ATTGATTTAA TATCTGTGTA GAAGCCAGCA AAATTGCTGT TTACTTATCC 240
TGTAGCTTCT GAGTGTCTTC TTTGCCCCTT TGCTCTCTCT CTTCCCCCTG TTACAGGCTA 300
TAGATATGAT TAAGAAAGAT CTATGTAATG GTGTTAAGTT ACTACACTCT TTGGAGGAGA 360
GATTTCTGGG GACAGGCCTG CGATAAGGGT GAGAGGAGTT GGATCCAGTC GTGAGAGTCA 420
GATAGGCAGC TCACCCACAC ACAACCTCTC CACAAGCGAG ACAGCTTCCC GGCCTTTCTT 480
GCTTGTTTTA ATCTGTGAAT GTTTCCCAGA AAGAAATAGT AACTTCTTTT TCTGGCAGGG 540
GTGCCTCCTG AAACTCCCTG AAAACAGGGC CTCTCCCTCC CCTTCAGGCT GGCCTCACAC 600
ATGCTAATGC AAATCAGTCC TGACCCAGCC AGGGGTCTTT GGGAAGGCTG CCAGGAGCTT 660
TAGAACAAAC ACGCGAAGAA TGTTATTTCA TTTCTGGCAT CCCGGGGAAA GAGGGACAGA 720
GAAGGAAGTT GGGCAGTAAA GGGGGTGGAG GGAGGGGGGA ATTCATATGA ATGCTTACTG 780
CAATAAGAGT GAAGCAAATG GAAAGGACAG CAGGAAATTC TTAGGAATAA AGGGCCTACT 840
AGGTGCCAGA AATGGACATA TGGAATATTT GGTTTTAATT TCACACATAC ACTCTGAAGA 900
AGAATTTATT ACTCTCACTT TTTGGATGCA GGAAGAGGCT TGGTCTCCAA GGTTAGGCAA 960
TTTTTCAAAG GCTACCCAGC TAAGAACTGA GGGAGTCAGA ATTTGAAACC AGATTTTTAC 1020
ATTTCAAACC TTGGGCTCTG TCTTCTCACT AAGGCTGGCT TACTGGTTGT GCTTTGATAG 1080
ATTCCCAACA AAACCCGCGA GTGCAACAGC CCCACATGCC ATGACCTCCA TCGTCTGTCT 1140
CCTCCTTTCC AGCCCCCTGC ATGGTTCTAA TTCCAGATTC ATTCAGCCAG ACCCCGAGCT 1200
AGTCTCCCTA CCTGCAGTCT CCTCTATTCT AACTTATACA CCACGAAGAT CTTTCTATAA 1260
CCCAACTGTG GCCTTATCAC TGCTCCTCCT TAGCACACGT TATGAGGCCT TGCAAGTCCT 1320
GCCTCTCCAA CCTCATATAC TGTACATTTC AACTGCCCTG AATCTCTGTT GTACCCCATA 1380
TGTGGTCCCT TCAATATCCT ACCTCCCTGC CTTCATTTCA GCTATTCCTT CTGCCTGTGA 1440
TGCAATAACT TCCCCAGTTC TAAGTGTTCA ATGCTATCCA TTCTTCCAGA CCTAGCTCAA 1500
AGGCACCTCC CCAAAGGCAC ACTAGCTGTT AGAGATCACA GCCTCCTCAG AACTCGCATG 1560
CCTTTATTAT GGGGCAAATC ACCTTCTACC CCCAATATGA TTAGCTGCTT AAAAGTTTGT 1620
CCCTAACACT 1630
|
