| Tag | Content |
|---|
EnhancerAtlas ID | HS187-04201 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr11:17007580-17009120 |
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 | | ZNF263 | MA0528.1 | chr11:17008941-17008962 | GCTCCCTCCTTTTCCTCCTTA | - | 6.37 | | ZNF740 | MA0753.2 | chr11:17008805-17008818 | CCACACCCCCCAC | + | 6.03 |
|
| | Number of super-enhancer constituents: 10 | 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_42048 | chr11:17008809-17010048 | 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 | ATGGAAGGGG GCATTCCTAC AAAAGCAAAG ACAAAGAAGC AAGAGAGTGC TACAGCTTAT 60
GATGTTGTGG AGTGTGTTCA GGCCAGAGGG GAATGGTGTG CTTTAACAGG ACACAGACAC 120
AGGAAGAGAA GCCCAAGTCA GGACACCTCT GAAGGCCCTC ATCAGGAAGC ATATCAGGAT 180
GAGGTATTTG GGCCCCTGTA GGGAGAACAG GATGGAGGCA AGAAAACCAG TCGGAACCAT 240
CTGCACCGCT GCAGATATGA GTTGGTGACA GTGGGGTCTT TAGGAGGCAC CAGAGAAAGG 300
ACTAATCACA AGAATCTGTT ACAAATCACA GGTGCAAGAC CCCATGGAGA AGGGAGGCAT 360
CGAATGAGCC CAGACACATT TTGAGTACAT AAGAAAAGTG CAGCCCCACC AGAGCCCTCC 420
TGGGAATGCT GCAAAGCTGC TGGGGAGATG CCAGCAGAAC CATGTCACAC CTTGCCCACA 480
GTCACCAAAG TGGGGACCCT ACTGACTGGC TGGAGGCAAG GAGGAAGTCA GGGGAGAGAA 540
ACCATAAAAA TTGCTCACTA TTTATTTCAC TTTCACTTTG AGCACACAAG TGGGGAGAAG 600
ACGCCCTGGC CCAGGAGTAG AGAAACCTGG CTGGAGTCCC AGCTGTCACC AACAACCTGA 660
GTAACCTTGG GCAGGTGACT TCACCGCTGG GGCTCAGCTT CCCCATCTAT AAACCAGAGC 720
TTCCACCATG AGCCCCACCT CTACCAACAT CCTGGAAAGG CCCCAATCAG ATAAGTATCA 780
GCTCTGCATA GCTTTATGTA GCACCTACTA TATGATCTTC CTTGTACCAG GAAGGGAGGC 840
AGGAAAGGGG CAGGCCGAGC CCCTGCCCAG AGAAGGTTTT AACAAGGTGG TCCAAGCAGG 900
TACTGCAGAA CACCGGCAAG GGCATTTCCA GCCACATTCT CCAGCCAGTC TTACTGCCCA 960
GCCCAACCCA GCCCAGGGAA GGCGGAGAGG AAGCAGTGAG CTGTTTTACA ATCCATCAAA 1020
TTAATTGCCC CAAATGGGAA ATTTGCAGGC CTCCTACAGC CTCCTGTGTA TTCCATAATC 1080
TCCCATGGCC CTAATCTGCT GAGAAAGAAT GTGTGGGCTG TAATCTTTTC AGCCCACTGT 1140
TCACAGGGGC AATGCCTTGG AAAAACCTCA GTCCCCACCA GTGATCACTC CCTCCCAACC 1200
AAAAGCCTCC CCGACCTCCC ATCCCCCACA CCCCCCACTG ACCTGGTGGC CAGCCAAGGC 1260
CTGGCTCCGC CCCCCAGAAG CCAGCTAGGC CAACCTTGGC CTTGACTTTG ACCTCGGAAA 1320
GGAGACCTGC CCAACCAGCT CCTTTGGTAA ATACAACTTT TGCTCCCTCC TTTTCCTCCT 1380
TAAGACAGAA CAGCCTGGCA GGAGGCAGAA CCAGGAGAAA TGGCTTCCGA GTAGAGACGC 1440
ACCCTTGAGG CGTGGTGAAA ACAGCCCCAG GTGAGGTGCT GGGCATTGGT TCTAACCTTT 1500
GCTTACCCTA TCCCTGCTAG GAAACCCACT TCCCATCTCT 1540
|
