| Tag | Content |
|---|
EnhancerAtlas ID | HS034-06046 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:121799730-121801290 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:121800011-121800032 | GGGGAAGGGGAGGGGAGGAGG | + | 6.07 | | ZNF263 | MA0528.1 | chr11:121800591-121800612 | GAAGGAGGGGAAGGCGGGGTG | + | 6.19 | | ZNF263 | MA0528.1 | chr11:121800010-121800031 | GGGGGAAGGGGAGGGGAGGAG | + | 6.52 | | ZNF263 | MA0528.1 | chr11:121799746-121799767 | GGGGGATGGGGAGGATGAGAA | + | 6.84 | | ZNF263 | MA0528.1 | chr11:121799738-121799759 | GGAGGAGAGGGGGATGGGGAG | + | 6.92 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I121928 | chr11 | 121799358 | 121801624 |
|
Enhancer Sequence | GTGAGTGTGG AGGAGAGGGG GATGGGGAGG ATGAGAAGAG ACACATACTG AGAGGCCTGC 60
AGGAGAAAAC TGGACCCAGG ACGCCCCAGA TTTGGCCACA CCAGCAGGGC AGTTAAAGGG 120
TCCTTTCTTG CTGGTAGGAA CGTCTAGTGC CAGGACCCCA CCCTCCCCCA CTCCCTTTTA 180
ATTCAATGGC TACGTAGGGG CTTCTTTGAT GGAGGCTTTG AAGTCGGTGG CTTTGAGATT 240
ACTCTTCCTC TGTGACCTTG ACCACCAGCC ATGAGGTTAG GGGGGAAGGG GAGGGGAGGA 300
GGAAGGCGCT GGAGTTGGAA AAAGGAAAGG AAAGAGAGGG GAGGGGAAGG AAGGCCGCCC 360
TAAGACATTT CTGCAGCATT CCACGACTTT TCTGATCACT CTGCAAAGTT GAAATATGAT 420
TGCAGCCTTT GCACCGGGAA GGAAAGAAAC CATTTAAATG AAAAATTAGC TGCCTTAGCA 480
GGTCAAGCAC ATAGTTACAT TAATGTCGTG TAGAACAATA AATCAACTTC GATCTCCAAT 540
TGAAAAAATG CTAATTTAGC TCAGCGATTC ACTGATTGTA CTTTCCTCTG ATAGAAATCT 600
TTTCTTTTAT TTAATGCGAA GCCGTGATTT GACAGCCTCC TCTAATGGTG CTTGCAGACT 660
CTCAGCATTT CAGTGGAATT CTGATCATGG TTTTAATATT CCGTGCAGCT CTGCCCCCTC 720
TGATTTCACG CTCACACATT AACGAGAGCT GACACTGGAG ATTAGACGCA GACAGCTGGA 780
ATGCCAGGTC TTTGTTGCAG CATGGACAGG AGCCAACGTC GTTCAACCAC AGCCAAGAGG 840
GACCTGGGAA AGTCTTCTTA AGAAGGAGGG GAAGGCGGGG TGGGGGGCTT GAGGGAGGGT 900
GGGAGCGGGG GATGGGAGCA AAAAGAAAGG CAAGGTAGTT TCTGAAGGGC ATATGAAAAT 960
AGATGTTTTC AGAAAGCCCT TTCGTCTCTG AAATTCACAT TGGAATCAAT TCTGGTTTAT 1020
TTAGAGGAAG TGGTTCATTA CAGGGAAATC CCAAATTGGT TGCAGTATTT TTCTGTAAAC 1080
TCTGAAAATA CAAGTGTGAT GCACGAAAAT GGAAATGGCT CCTGCTTCAG CTGCTCACTA 1140
GTTCGTCTGA GAAACAATGG TGATTACGAG CTGGAGGAAG AGTGCTTACA TAAGGAAATG 1200
TGTTCTCCCC TTTGCCTTAA AAAAAATCAC TTAGTTCCAG GTGAATAGAT GGGGAAATAA 1260
AACGAGATTT ATGAGCCAGG GCTGCCTGTG CGACTAGCGA CTACCTCGGC AAGAAAGGAA 1320
GTCGCGTAGC CTAACTGCCT TGATCCTCAT AAATTGTTTC CTGATACCAG AAATCAAATA 1380
AAGATCCATA GTTTCATCTA AACCATAAAG CCACTTGGGC TCAGCTAGTG CCGATATTGC 1440
AAAGGGGAAG GAAGGGTGCT GCCTGAGACA CTGGCTCAAC TTTGTCCGAA AGAAGATGAC 1500
AGATGACCAA AGTTGCGGAG GCGGCGCATT AATACTATGT CAAAAAAAAT TGTTTCTGCT 1560
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