| Tag | Content |
|---|
EnhancerAtlas ID | HS101-34248 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:16811780-16814180 |
Target genes | |
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 | chr5:16813924-16813945 | AGTGGAGGAGAAGGAGGAAAG | + | 6.81 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I016811 | chr5 | 16811350 | 16814114 |
|
Enhancer Sequence | CCTGAGTAGA AGGGACTACA GGGGCACGCC ACCACGGCTG GCTAATTTTT GCAATCTTTT 60
GTAGAGATGG GACTTCGCCA AATTGCCCAG GCTTGTCTTG AACTCATGGG CTCAAGCGAT 120
CCTCCCGCCT CAGCCTCCCA AAGAGCTGGG ATTACAAGCA TGAGCCACCA TGCCAGGCTT 180
TCTACTCAAC CCTGATTGAT CTCATGCCTT TGTAGCGTCA CCACCACCAC CACCTCCATA 240
GGGCTTCCTG AGCCACACAT AGGTTATGTC TCTGTACCAC AAACACATAC CCTGCTCCTC 300
CTCTCCTTAG CGGGTATTTG CCCTTGCCAG GTCTTAGCAG GCGGTGACAG GAGATGAAGA 360
AGTCTAGGCC CTCATCAGAC CCATTCCAAG GAAGGGGACA ATCAGGAGAG AGCCAACCCC 420
CTCTCCTCAA GGCAGCAAAC CCATAGCCAA GAGGTTCAGG GTGGAAACCT GGGGCCCCTG 480
GCTGGGAACT GGGAGCAGAG CAGGGCTCTA GTCTTGAAGT GGCCAGAGGA AGGATAAGAT 540
TGATGAGGGG AAGTCTCAGG CAGGAAGAGC CTGGGGTTCC AGGAAGAGAA TCTAACAGGG 600
GCATAGAAGG CCGGGCTTCT GCACAGGCAG TTACAGCCAG CGCAGAGGGG CTCTAACCCA 660
GGCACTGCAG CTTAAACCAC GCAGTCCAGA CCTATGGACA CTGGCATCAA ACTCGGTACG 720
GCCTCTGTCC CCTCAGCGAC AAGCCTGGGA CAGGAATGCA CCCACAGGAA TAGCTAAAGG 780
GCCCAGCGGT AAGGTTCAGG GGCTTCATAA GCACACTCAA ACCCAAGCCT GTGTCATCAT 840
CACATAACCC TCAATGACAG GACTTCAGCT ATCCAAGGCC ATGTGCTGTG AGCTGGCCTT 900
GGTGTTATCT CCCCACTAAA TTGCAAGCTT TGAGGCTAGG GATGATGCTG TAAACTTCTT 960
CCAAATCCCC CTTAAAATGG AGCCAAGTTC GAGGCAGGAA CTTTCTAAAT AAACACTTGT 1020
TGCTATGAGA TGGCTAAGAT GGAGACAAAG GTACAAAGGT TAAAGTTCCC AGAGCTTTCA 1080
CTTCTTTTAC TTTAAAACAT CCCTGTTAAG AGGGATTATG ATATCTGACC TTTGAAAACA 1140
CGTTTATTTT AAAAACTGGT GTTCAGAAAG ATTCAATTAT CAATACGGAG CCAAAGAGGA 1200
GGTTAGTGAA GAAAAGGGAA GATCAACTCT AACTTGACTA TTCTGGGTGC TTTTATTTTT 1260
TTTTTTTTTT TATCACTTTC TACCCCATTT CAATAGAAGA TGCCAAAAGC TACAATAAAA 1320
AAATATTTTC CTGGTTTCTG ACAAAGTTCT CAGATAAAAA GACCAGTCCC CAAGGAGAAA 1380
AAGCTAACAT TACTCCTTAG CAAAGAATGG CAGCCTCTCT ACCTGGCGAT GAGCCACTTG 1440
CCAGCAACCC ATGGAACCTG ACAGCTCAGA ACAGAAAGTC AACAAATAAT GAAACATCCA 1500
GACGCCAGCA GGGGGAAAAT GCCACAGGAG TCCCTCCTCA ATGATATGAC TCAAAGGAGA 1560
GTACCTGGCT GGATGCGGAG GCTCATGCCT GTCATCCCAA CACGTTGGAA GGCCCAGGAG 1620
GGAGGATCAC TTGAGCCCAG GAGTTCAAGA CCAGCCTGTG CAACATAGCA ATGTTTTATA 1680
AATTTAAAAA AATTAAAAAA ACTTAAAAAT TAACCAAGTG CAGTGGCTCA CACCTATAGT 1740
CCTATATATT ATATACTGTA GTACTATATA TATACTCAGG CGAGAGGATC ACTGGAGCCC 1800
AGGAGTGAGT TAGAGGCTGC AGGGAACAGC GATCATGTCA CTGCATTCCA GCCCAGGAGA 1860
CAAAGTGAGA CCCTGGCTCT AAAAAAAAAA AAAAACCAAC AACAACAAAA AAAGGAGGAC 1920
ACGTATGGTG GGCAGAATAA TGGCTCCTCC CGCAAAGACA TCCATCCACA CTCATCCCAG 1980
AGCCTGTGAC TAGATAATGT CACATGGCAA AGGGGCTCTG CACAGGTGAT TATGGTTATG 2040
AAGCCTGAGA TGGGGAGATC ATCCAGGGAG GCCCAATCTA ATCATGTGAG GCCTTAAAAG 2100
CAGACAGCCT TTCTTGGCTG CAGTCAGAGA GAGAGAAAGA AGACAGTGGA GGAGAAGGAG 2160
GAAAGATTTG AAGCCATGAG AGGGAAACAA TACATGGTTA CTGGCACTGA AGATGAAGAA 2220
AGGGAGCCAC AGATCAGGAG ACCAGGGAAT GTGAGCGGCC TCTAGAAGCT GGGAACAGCC 2280
CTCAGGTGAC AGTCAGCAAG AAAACAAGGA CCTCAGTCCT CCAACTGCAA GTAACTGAAT 2340
TCAGCCAACG ACACAATGAG CAGGAAACGG ATCCTCCTCT AGAGCATCTG GAAACAGACG 2400
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