| Tag | Content |
|---|
EnhancerAtlas ID | HS101-07361 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:34668230-34670560 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr11:34669306-34669319 | TAGATGATGTCAT | + | 7.12 | | JUND(var.2) | MA0492.1 | chr11:34669305-34669320 | TTAGATGATGTCATT | + | 6.58 | | RREB1 | MA0073.1 | chr11:34668634-34668654 | CCCCCACACACACACACAAA | + | 6.05 | | RREB1 | MA0073.1 | chr11:34668632-34668652 | CCCCCCCACACACACACACA | + | 6.17 | | Twist2 | MA0633.1 | chr11:34668804-34668814 | AACATATGGT | - | 6.02 | | ZBTB18 | MA0698.1 | chr11:34668921-34668934 | ATTCCAGATGTTG | + | 6.28 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_26655 | chr11:34668716-34669787 | Esophagus | | SE_26655 | chr11:34670108-34673600 | Esophagus | | SE_31738 | chr11:34668971-34669471 | Gastric | | SE_41618 | chr11:34668933-34669424 | LNCaP | | SE_41618 | chr11:34669465-34669700 | LNCaP | | SE_56256 | chr11:34665026-34669543 | u87 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH11I034648 | chr11 | 34670342 | 34671085 | | GH11I034638 | chr11 | 34659831 | 34669583 |
|
Enhancer Sequence | GGTGACTCTC TCTTTCTGTG TCTCTCCCTA CCCTGCTAGG AGCCAGCTGG AAGAATAGAG 60
ATTCTGCAGA TGACAGGATT CTTTGTCAGG GACAAGAAAG AGTGGTCTCA CCTCCAAATT 120
ACCATGTCCC AAGACAGAGA AATGGAAGGA AGATGAAAGG ACAGGATTGA AGCATAGGGT 180
ACCTGGTGTG CCTAATCCCT TATAAATGCC AGTGTAATTT AATTCTTTCC TTATGGTGAT 240
AATTTTCAAG AAGACAAAAG CTGGCTAGGA ATTCGTAGAA TACTTACTAT CCTTGGAAAA 300
TGTTTTCTTT CCTTTGCAAA CAGTCCAGTC ACTTGCTTGT TAAAAAGATC ATCATGGTTA 360
CAAAAAAAAA AACAAAAAAC AAAAAACAAA ACAAAACAAA ACCCCCCCCA CACACACACA 420
CAAAGAACCT TCTAGACCTA GGTTCTTAAG ATAGGGTCCT AAGGGTGGTA AGAAGATATA 480
TGAAATTAGA ACTATGTTTG TGTTTTGGGA GGGGAAAAAA CTCACAATAC TTCAGCAGAT 540
TCTTAAAAGG TCTGTAACTT AAAAAAAGGG TTAGAACATA TGGTCTAGAC ACGTGTATGG 600
GGAATGTTTC TGTGGTGGTT TCTGGAATTT CTGTTGCCCT AATGCCCCAG ATGTCTCTCT 660
GAGGCTTCCC CTAGCACAGG GATGGGCCAC CATTCCAGAT GTTGTCTTTG AGTGGTAGAT 720
TATTCATACA CGAACATATC CTATACTGAC ATGTAAGACC TAGTAGGGTG GACAACTGAC 780
CTTGCAGAAT GGTTTTGACA CTGGCATAAG GTTCCCCTGA TAGTGGCTGT AAAAATCTAG 840
CTCTTCTGAG AACTATGGGC ATCCTGAAAA GTAGCAATAT TTAAGAACAG GGAGTTGGCC 900
TGTCTGCACT GGAAAAGGCA TTTATGTCTT GGTAGAACCC ATGTTTGGGC AAGTAACCGG 960
GACTTGGGCG GCATGAGCTC CAGGGCTGTG AACCAGAGTC ATACCCTGGC AACAGCCATC 1020
AACACTGAAG AGGACCTGGG GCCTTGCAGC AGAGCTTGTG GCTGCGGTGG CCATTTTAGA 1080
TGATGTCATT CAGCTCCCTG GCCATGCCCT GCTTCCCACC CACCTCACAT TGGTGGCTGC 1140
TCTTTTTTCT TTGACTAGAA TCAAACCAAA CAAGGCTCTA TAAATAACCC TCAGGGATCT 1200
TCAAAAAGAT CAGACTTACA CTTGAAGAAT TAAAAATATT TACCTCCACC CCCCAATTAA 1260
ATCCACTCCT TTAAAGCTTT GCCCTGATTG AGGTCTGAGG CAGGGAGGCC TGGGAGGTGC 1320
TGTGGCCATC TTAGACCTTC TGTCTCTGAC TTCCCATGAC TTGTTTGGTC TCATCGCATG 1380
CTGCTGTAGC CTCTGAGTTC CTAATGTCCA GGCAGATTGC TCACTCTTTT GTTGTTTGCC 1440
TTTGTGTAGA CCTTCTATCA ACTAACATTT ATTGAGTATT TACTTATACT AGGCACTGTA 1500
AGTGAATTAA TTCATTTAAT AACTTTATGA CAAAGTAAAT ATTGTGCCCA TTTTACAGGT 1560
GGGAAGACTG AATGTCAGAG AGGTTAAAGG CATGGCTTCT GTTCTTGAGA TGTTTAGAAT 1620
CTGTCTGGGG AAGAAAACAG ACTAGATTCA TATGCATTTA CAAATATATA TATATATATA 1680
TAAGCATACA TATATATGCT TTTATATATG ATAATGGGAG AGGAGTTGCA AGCAAACAAG 1740
GTCATGTGAT GTGTACTGCT TGTACATGTG CTGAGGCATA AATAAGGAAA GAGTCACCAC 1800
ATTTTATCCA GACATATCTC ACAGATTGGA TGTAATCATG ATGGCATTGA TTAGATTTTA 1860
AATCAAAGAA GAATCAAGCT AGTTAAAAAG GTTTTTCCCT ACATTTTCAT TTTCATATCA 1920
TATCTTAGTA TGGGAAAGCA CCTTAGAAGT CATCTAGTGA CCTTATCTAG TTTAATCTTG 1980
TTACAGATGG GGAAACTGAG ACCCAGAAAG GTAAAGTGCA CACACCTTCC TCATAGCTAG 2040
TAGTTGAAAA ACTGGGCTTC TGAAGTTCTA TTTCCACCAT ACTGAATGCC TTTACTATAC 2100
CACATCAAAT AATTGCTTCT AAGGTAGTGC CTTAGATTCC CAATTTTCTG GGGTCAGAGA 2160
CTGCAGGCTT GAGTTTGTAG AGGCTGACAG AGAAACCACC TCCCATAAAC AAACATAGGT 2220
GACCAGGCAG TAGGATGGCA GAAGCTCTGC AAAGATGCCA GTTCTGTCCT TATTTAAGCA 2280
TCCAGTTCTG GCTCCATCTG GGCCCTCTCT GACTATCCCA ATCTGTCCTT 2330
|
