| Tag | Content |
|---|
EnhancerAtlas ID | HS101-06906 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:12116220-12118060 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:12116605-12116623 | GGGAGGAAGGAAGCAGGC | + | 6.35 | | EWSR1-FLI1 | MA0149.1 | chr11:12116601-12116619 | GGGAGGGAGGAAGGAAGC | + | 7.39 | | EWSR1-FLI1 | MA0149.1 | chr11:12116597-12116615 | GAAAGGGAGGGAGGAAGG | + | 7.45 | | Gata1 | MA0035.3 | chr11:12116650-12116661 | ACAGATAAGGA | - | 6.14 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_23124 | chr11:12116298-12118124 | Colon_Crypt_1 | | SE_24571 | chr11:12116461-12117419 | Colon_Crypt_2 | | SE_42113 | chr11:12116311-12117543 | Lung | | SE_49900 | chr11:12116311-12119216 | RPMI-8402 | | SE_50078 | chr11:12116240-12118222 | Sigmoid_Colon | | SE_52873 | chr11:12116247-12117510 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I012094 | chr11 | 12116061 | 12117502 |
|
Enhancer Sequence | TAATATTATT TTATATATAT ATATACACAC ACAAAAATTA GCCAGGTGTG ATGGCAGGCA 60
CCTGCAGTCC CAGCTACTCG GGAGGGTGAG GCAGGAGAAT CGCTTAAACT CAGGAGACAG 120
AGGTTGCAGT GAGCTGAGGT CACACCACTG CACTCCAGCC TGGGCGAAAG AGCAAAACTC 180
TGTCTCAAAA AAATAAATGA ATAAGAAAAA AAGAAAAGAA AAAGAAAAAC TCAGCTACAA 240
CAGAGTGACT GGTTATAATT TCCCTGCAAA ACTGCTAATT CTCTGATGGA GGGACAAGCG 300
CTGAATCAGG TTTTGTTTAT CTCTGCAGAG TACCTACATT GTTCCCTCTT ATGATAGGAG 360
CTCAAACACA TGTTGATGAA AGGGAGGGAG GAAGGAAGCA GGCAGGCCCG CAGGCCCATG 420
CCCTTCTTTT ACAGATAAGG AGACAGAGCT GGGACGGGTG GAGGAGTGTT CAAGGACATT 480
CTTGGCTAGA AACTTACTAT CTAAAATAGT AAAGAGACCT CTAACCATTC TGCTGACAAA 540
CTTATAAGCA CAATAAGCTT TGAATAACAA ACACTCCGCA GGTAAAGTTC CATGACAACG 600
ATTCTTGTTA TAAAGTTGTG GTCTTCATAG AGAAGTGCTT TCCTCTCTCA GGCAGGAAAA 660
GAGTTCCTTT AAAATAGATC GAAATGCTCT GTGATGAATA ATACGAAGCA GTAAGGCCTT 720
CACCTGGCCT GGGTCCAAAT AACAGGTTCT ATTCAGGTGG CTCTGAAAGC ACCTGATTGT 780
GTGCTGTCGC CACTGTGGGC AGGGCAAGTC CAGCAGAACT TTACAAGTCT TTTGTTCTGC 840
CAGCAAGCAG TAATTGGTTC TCCACCCCAG TGTAGTAAAC TTCCAGCCAC CTGAATGAAA 900
TTCACCTAAT TTAACAAACT GCACGAGAAG CAAAGCAACT CCCGGAGCAT ACACAGGTGT 960
GAATATTGTG CATCTGTCTT CTCTGTGATT CCTCTTGTCT TGAGGCTTCC ACACCCCTCT 1020
GGTCCTTGGT TCGTCCTGTC CCCTCTTCTC CAGACCCATC TTCCCATCTA CTGCAGACCT 1080
GGCTCTATTG GGTATTGAAT CTGCTTCTCT CCACACCTCA GTTTCCCCCT TTCACCTAGC 1140
TCTTCCTTTT AGCTTCTAAA CATGCTCAAG GCTTGCAGCC TAAAAATGAA AATACTACAA 1200
ACTACTCTTT ATTCTGCTTC TTCCCCCACT GTGTGCCCCT TCCAGTCATA AGCGATTCTG 1260
CAAGGAACCA TCTATACTCA GTCTCTACCA TCTCATTTCT TGCTACATAG CAAACAACGT 1320
TCTAAGAATT TTACATATAT TGACTTATGG AAGCCTGACA ACATCACTGT GATGTAAGTG 1380
CTATTGTTAT TTACATTTTA TGGATGAGGA CAAGGAGGCA CTGAACAGCA AAGTATTTGC 1440
CCTGGATCAC CAGGATTTGG GCAAAGGTAT GCTCTGAGAC CTTTTTCCCC GCCTTATGCC 1500
CATTACAAGG TACCTTGAAT GAAAAAATAC ACAAGAACAT TGCATGGACC TGTCTCATTT 1560
ATTGATTCAT TCATTTCTTC ATTATTTAAC ACTTACTGGA GGCCTACCAT GTGCAAGACA 1620
AGAGAAAGAC ATGAGTCTGC TGTTGACATG GTCAGAGTCC AAAATGGGAG GCAGGCCTGC 1680
AATATAGCAT AAGAAGAGCT CTGGTAAATA GGTGACAGGG GGCTAGGGAA GCCCAAAGGA 1740
AGCAGCTCAC TTTGCTCATA GCGGTGGTTC CCGAATTTCA CCATGCATTG GAATCACCTG 1800
AGATCTTTCA AAACTACCAA TTCCTGCCTC CCACCCCAAG 1840
|
