| Tag | Content |
|---|
EnhancerAtlas ID | HS092-02910 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:113064470-113066140 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr1:113064542-113064553 | AAATCACAGCT | + | 6.14 | | ZNF263 | MA0528.1 | chr1:113065502-113065523 | TAAGGAGGGGGAAATGGGAGG | + | 6.26 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I112522 | chr1 | 113064733 | 113068448 |
|
Enhancer Sequence | ATCTTTTGCC TGTTGATATC TTAAAGCAGC AGAGTGGTAT AGAAATTTGC GGTTATGACA 60
GACCCGGGTT AAAAATCACA GCTGTGCCAT TTGCTTTGAT ATTTTGAGCA AGGTAGCTAA 120
ATTTTCTGAG CTTCTATTTT CTCATCTGTA AAATGAGGAT ACGTACCTGT TCTTTTTTTT 180
CTTTCTTTTT ATTTCTTTTA GAGATAGGGT CTCGCTTTGT TGCCCAGGCT GGAGTGCACT 240
GGCATGATCA TGGCTCACTG CAGCCTCAAA TTCCCAGGCT CAAGCAATCC TCCCACCTCA 300
GCCTCCCCAT TAGCTGGGAC TACAGGGCCA TGCCATCATG CCCAGCTAAT TTAAACATAG 360
TTTTCAGAGA TGGAGCTCAC TATGTTGCCC AGGCTGGTCT TGAATTCTTG GTCTCAAGCA 420
ATCCTCCCAC TGCAGCCTTC CAAAGTGCTG GGCGTACAAG CGCAAGCCAC TGTGCCCAGC 480
TGTCAGACGC TGAGTTTTAA TTATGCACCA AACTCCAGCC CGCAGATCCT CTTCACCAAA 540
GCCCCTGGCT GGTCTAGCCC ATCATGACTT CTCTAGGAAC AGTCCTTCTT TAGGACTATA 600
AAGTATTAAC AAAAGTCTGT AGATTAAGGA GCCTGCATAA AGAATTCTGG ATACAGGCCC 660
CTGTCTTTCC AAAGTTCCTC TCCAATATCC CTTGGGGTCC TCATGTTTTT GAAGCAGCTT 720
CACTCTGCAC AGGCAGCAGG AGGTTGGGGG AGCCATAGCT CTGGGCCACG GGGGCAGATT 780
TATTTGGATG ATAGGACTAA TATTTGTGTA ACCTGCTGAG ACCTGTGTGG GAGAGTTTAG 840
GGTGGTTTTT CTTTTGGTGA GGGGATTTGC TCTGGTTTCA CATCCATTAA CACAAAACAT 900
GAGCTAGTCA GGGCCCTTGT GGTCTGCGGT AAGGGGATGC CTGTGGAGAA ATGGGCCTGA 960
GTGAGTCAGG CCAAGAGAAT GTCTTCCTTC AGAATGGAGT CAACTGGATA ACTGATGAGC 1020
CAATGGTGGG ATTAAGGAGG GGGAAATGGG AGGGGAAGAG AACAGCTGAC ATCTTGAGGA 1080
AAGCTTTGGG GTAGTGGAGA GGTAAGGGGG TCATGGTCAG TCTGAACTCA ACAATAGGGC 1140
TGAATGAATT TACCAAAGGA AGCTGCCTTA TATTATATGC CAGGCTGCTG GGGAAAGCCT 1200
CAGGTCCTGG CCAGCCCCTG TTCTCACAAG AACATGCAGG TTACCACATA AATAATGGCA 1260
TATGCCTTCC ATAGGACGTC AACCTGACTT AAATCTACCT ATACCCTACT CTCTATTCTT 1320
TGGTTTTTGG TTCTCATCCC TGTGGAAGGA AATGGGCCTC TTCTGGCATC TCATGCTACT 1380
CTGTGCTTTT CCTTGGGCTC CAAATTCTAG CTCATAAAGA TGCAAGTTTT GCAATTTCCT 1440
ATAAATGGTT AAGAAAAGAG CAAGCTGTCC AGAGAGTGAG AAGTTTGAAA AGAGAGGTGC 1500
ATAAGAGAGA AATGATGTCC ATTTGAGCCC CACCACGGAG GTTATGTGGT CCCAAAAGGA 1560
ATGATGGCCA AGCAATTAAT TTTTCCTCCT AGTTCTTAGC TTGCTTCTGC ATTGATTGGC 1620
TTTACACAAC TGGCATTTAG TCTGCATTAC ACAAATAGAC ACTAATTTAT 1670
|
