| Tag | Content |
|---|
EnhancerAtlas ID | HS170-00675 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr11:94986990-94988420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr11:94988086-94988096 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr11:94988086-94988096 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr11:94988086-94988096 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr11:94988086-94988096 | AACAGCTGTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_09975 | chr11:94986531-94990907 | CD14 | | SE_10597 | chr11:94985364-94991092 | CD19_Primary | | SE_11552 | chr11:94985143-94991621 | CD20 | | SE_29469 | chr11:94985943-94988563 | Fetal_Intestine_Large | | SE_33313 | chr11:94988016-94990033 | H1 | | SE_62584 | chr11:94960773-94991031 | Tonsil | | SE_63441 | chr11:94962357-94990341 | NCI-H69 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I095252 | chr11 | 94985491 | 94990919 |
|
Enhancer Sequence | GGGAAGTAAT AGTACCTCAT GCATGGGACA GCTGCAAAGA ACATATGAGA CATTGTATAT 60
AAAAAAGTTC TTTGCGCACT GTAAAGGGCA ACAGACAAGT TGGCCTTTGT CACTACTTCC 120
CCAGTTTACC TAAGGCTTAC AGAATGCTGG GAAAATAAAT GAGAGGTAAT AAGGCATTTT 180
TTATAGAAAG TCCTAAAAAT TACTTCACAA TTCTTTGCAG CAAGTGAAGA CATAGTTTAA 240
TACTGATGGT AAAGGCAAAT GAACTAATCA GAAGGCCAGC CCCATCTAGG AGATGTGTAA 300
GACATCTTCC ACCTACAGTC GAAGGCAAAC GATAAGGTTT TTTTCTTATT CTCTTGTATT 360
CTAGAGGCTG TTGGGGGTTG GGTGGCTTGG AAGAGAAAGT GCCACACAAT AGCATTTGCT 420
AGATTACGGC ATGGGGGTTG GGAGGGCGCT ATAATTTAAG AGGCATAAGA TGACTGAAGT 480
GATCACACAA AAAAGATATC TTCCAATTCC ATTTGAGCTA CAATCTGATT TCGCTGTTGA 540
GTACAACGTC CCCTTCACAA GAATCAGAAG TCAGCATCAG GGCTGTGCTG CATAAGTTTT 600
CCACCCAGCA ACAGGATGAT GTCAGCAGCC AGGGAGAACG ACCAATCAGC AGGCAGAATG 660
AATCAGAGCG TGCTGGGATT TTGCTCAACT GTCTCTTAGC AAAGCAAGCT GTGCTCTGAA 720
GTGCAGGGGT TATTTGCACT TCCTCTGCAC TTGAAGCTGA GGCTGAATGG CTCTTTAGCT 780
GAAAAGGTAC CAAGGAGTGT GCAAGCAGTT AAGATGATTT GCATCCAAGC AGCCAGTCTC 840
ATAAGTCATG AGTCATATTT GTTTTCCTGA AAGTATTTTT TTGGAATAAA AAATTCAGCA 900
TTAATAAAGA TTCTAAAGTC TTGATTTATA TGTTGTGTCT TATAATTGCT TGAAACCTGT 960
TTTGTTTCAT GCATAGTGAT GCTGGGCAGC TCTTGGCACA TGAGCTACAA GTAAAGTTCA 1020
ATACTGCCTC TTAGGGAGTT TGAACTTGCC TCTGATGTTT CAAGTCTTCT CTCTAATGAC 1080
AAGCAGCCTG GAAATCAACA GCTGTTTCAT TTCTGGGGCA AAAGTGCTAA TTCTCCAATT 1140
ACACTAAAGT GTGTTTTGTG TGTGCTTTAA AAATAAGTCT AAGCTGGAAG GATATGATGT 1200
GACTTGTAGA CATTGTCTCA TGGGTGGGAG TGGAGAGGGC TTTGTAGCAT TTCTGAAAAC 1260
ATGAAGTTAT TTCCCAAAAT TTTGTCAGTT TTTCTGATCT TAGTGGGCAG TGACAGCAGT 1320
ATTGGAAAAG GGTGCAATCG AAGGGTTAAA CCTACCTACC CGGCATTACC TATGACATAT 1380
CCCAGGTCGA TTAGACCTCC CAGGCAGGTT CCTCACTGGC ATTATCTGAG 1430
|
