| Tag | Content |
|---|
EnhancerAtlas ID | HS073-02214 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr11:17007570-17008620 |
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 | chr11:17008409-17008427 | GGAAGGGAGGCAGGAAAG | + | 7.67 | | IRF1 | MA0050.2 | chr11:17008138-17008159 | TATTTATTTCACTTTCACTTT | + | 6.96 | | PRDM1 | MA0508.2 | chr11:17008146-17008156 | TCACTTTCAC | + | 6.02 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_23209 | chr11:17006345-17010079 | Colon_Crypt_1 | | SE_24588 | chr11:17006954-17010047 | Colon_Crypt_2 | | SE_27642 | chr11:17005603-17011510 | Fetal_Intestine | | SE_28618 | chr11:17005858-17011943 | Fetal_Intestine_Large | | SE_31464 | chr11:17005871-17010093 | Gastric | | SE_42048 | chr11:17006935-17008802 | LNCaP | | SE_48027 | chr11:17007452-17009993 | Pancreas | | SE_50712 | chr11:17006304-17010109 | Sigmoid_Colon | | SE_52571 | chr11:17006346-17010116 | Small_Intestine |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I016978 | chr11 | 17000394 | 17011590 |
|
Enhancer Sequence | AATTACCTGG ATGGAAGGGG GCATTCCTAC AAAAGCAAAG ACAAAGAAGC AAGAGAGTGC 60
TACAGCTTAT GATGTTGTGG AGTGTGTTCA GGCCAGAGGG GAATGGTGTG CTTTAACAGG 120
ACACAGACAC AGGAAGAGAA GCCCAAGTCA GGACACCTCT GAAGGCCCTC ATCAGGAAGC 180
ATATCAGGAT GAGGTATTTG GGCCCCTGTA GGGAGAACAG GATGGAGGCA AGAAAACCAG 240
TCGGAACCAT CTGCACCGCT GCAGATATGA GTTGGTGACA GTGGGGTCTT TAGGAGGCAC 300
CAGAGAAAGG ACTAATCACA AGAATCTGTT ACAAATCACA GGTGCAAGAC CCCATGGAGA 360
AGGGAGGCAT CGAATGAGCC CAGACACATT TTGAGTACAT AAGAAAAGTG CAGCCCCACC 420
AGAGCCCTCC TGGGAATGCT GCAAAGCTGC TGGGGAGATG CCAGCAGAAC CATGTCACAC 480
CTTGCCCACA GTCACCAAAG TGGGGACCCT ACTGACTGGC TGGAGGCAAG GAGGAAGTCA 540
GGGGAGAGAA ACCATAAAAA TTGCTCACTA TTTATTTCAC TTTCACTTTG AGCACACAAG 600
TGGGGAGAAG ACGCCCTGGC CCAGGAGTAG AGAAACCTGG CTGGAGTCCC AGCTGTCACC 660
AACAACCTGA GTAACCTTGG GCAGGTGACT TCACCGCTGG GGCTCAGCTT CCCCATCTAT 720
AAACCAGAGC TTCCACCATG AGCCCCACCT CTACCAACAT CCTGGAAAGG CCCCAATCAG 780
ATAAGTATCA GCTCTGCATA GCTTTATGTA GCACCTACTA TATGATCTTC CTTGTACCAG 840
GAAGGGAGGC AGGAAAGGGG CAGGCCGAGC CCCTGCCCAG AGAAGGTTTT AACAAGGTGG 900
TCCAAGCAGG TACTGCAGAA CACCGGCAAG GGCATTTCCA GCCACATTCT CCAGCCAGTC 960
TTACTGCCCA GCCCAACCCA GCCCAGGGAA GGCGGAGAGG AAGCAGTGAG CTGTTTTACA 1020
ATCCATCAAA TTAATTGCCC CAAATGGGAA 1050
|
