| Tag | Content |
|---|
EnhancerAtlas ID | HS101-01561 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:51801240-51803080 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| POU4F2 | MA0683.1 | chr1:51801841-51801857 | CTCATTAATAATTCAC | - | 7.42 | | ZNF263 | MA0528.1 | chr1:51801409-51801430 | GGGGGAAGAAGAGAAGAAAGG | + | 6.76 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65473 | chr1:51801180-51802382 | Pancreatic_islets |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I051335 | chr1 | 51801181 | 51802382 |
|
Enhancer Sequence | AAAAAAAAAA AAAGAGCCCT TAATAAATAC CTATTAAGTG AGCCCTTAGA ATGCCCTAGA 60
AAGTTTGTAA TAGCATTACC TCCCATCCTA CAGATGAGAA AATAGAGGCT TGGACCAACA 120
TCTAGCCGTA GCTCGAACCC AGGTCTTGAT TCCTTATTCT CTAGGGAAAG GGGGAAGAAG 180
AGAAGAAAGG AGGGGTGTTT TAAGTGGGAG AGGTCATAGA AATGGGGGAT GCAAGCAGTG 240
ACACATGATG CCATTGTTGT AGAAAGAGCT TAAGCTGTGA AGTCAGTTCT GCCTCTACCT 300
CTCAGAACCT CAGTTTTCCC ATCTATAAAC CTGGGATAAT AATCCCAAAC TCTCAGGGAT 360
GCTGTGCAGA TTACTGAGCA TTATTTGGGT GACTCCTTCC CCCTTCTCAG CACCCCTCCC 420
AGCCCCTTCC CCCAGGCCTT TCCCTGGCAT GAAGCGCCCC CTCCCCAACA CCTGCAGTCT 480
CTGCCAGCCC AGATACCCCC TCTTCAGAGT CTAGAACCCT TCCTCTCTCA CTGAACTGGT 540
GACTGTAAAG CAGGTTTCCT TAAAGCGAGT GAGCCCCACC CTAACAGGTT ACAGGTTTGG 600
GCTCATTAAT AATTCACAAG TGAACAGGCC TGTCAACAAA GGGCCTTTGG AGGGCTGTGA 660
CAGTGACAGA TCTTAAATAT TCTCTGGCAA GGGCCCCTAA GGAAGGATCT ATTCCTGCTC 720
CTTGGGCAGG CATGGACTCT GCCCCCCGCT AGCTCTGTGA CCTTTGGCAA GTCACTGCCC 780
CACTGTGGGG CAGTTTCCTC TTCCCACCAG ATATAAAGGG GAGAGAAATT TGGGCCAAGA 840
ACTCATGGGC CCTCCCTGCT CTGAGGGTCT CTGTTCTAGG ATCTGGGCTC TTCTACCTAA 900
GTCTGGTCTC TAGGAGCTGC TGAAGGTAGG TCTAAAGAAG GAGCCTGGGT TAGCACAAGG 960
GACCAAGAAC AGCTCTAACT GAAAAAAGGG GTCAGAGCTC TAATGAGGGG TTTCCAGCAT 1020
TGATGGCAAC CTTTCAGGGG TCAGAACTTG GGATGCAAAG ACAGGAAGAT CTGGATGGAC 1080
TCCTGGCCCC ACTATGTCCT AGCTGGGCAG TCCCAAGCAA TTCATCCGAT TAGAGAATAG 1140
TTCAGAGAGC AGGTTTGAAA GCCAGGGCTT GCACCTGACA CCCTGGGCCA GTAACTTCAT 1200
TTCTGAAACG GGGATGATGA TGGCACCAAC CTCATTAGGT TGTTGCAAGG ATTAAATGAG 1260
CTACATATCT TCAGGGCAGA TGAGCTACCT GACACACTGC TGGTGACAAT AGAAATTGGC 1320
TCCATCTGCC TGTAATCCCA GCACTTTGAG AGGCCAAGGC GGGAGAATTG CTTGAGGCCA 1380
GAAGTTGGAG ACCAGCTTCA GCAACATAGT GAAACCCCCG TCTCTACAAA AAATAAAAAC 1440
TTAGCTGGGC ATGGTGGCAC ACAACCATAG TCTGCTACCG TCTATTATCC ACACAGCACC 1500
AGGCCCATTT GACACTTAGG CCAGATCACA TCACAACTCT GCTCAAAGCC CTGCAAAGGC 1560
TCCGCATGTT CCTCAGTGCA AAAACTAGTC TGTCTATGGC TCATGAGGCC CTGCACAACC 1620
TGTATGCTCC CATCATCTCC CGACATCATT TCCCTTTATT CCCTCTCTTA TTTCAGCCAC 1680
ACCAGCCTCC TTGCTCACCT CCAAATATGC CAGGCACATT CCCACCTCAG GCCCTTTGGA 1740
CTTGCTATTC CGTCTGCCTG GAATGCTCTT CTCACACGAT TCACTACTTC ACCTTCTTCG 1800
GGTCTCAGCT CAAATATCAC CTTCTCCGTG AGGCCTTCCC 1840
|
