| Tag | Content |
|---|
EnhancerAtlas ID | HS101-00691 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:23065740-23067360 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GRHL1 | MA0647.1 | chr1:23066545-23066557 | TAAACCGGTTTT | + | 6.44 | | GRHL1 | MA0647.1 | chr1:23066545-23066557 | TAAACCGGTTTT | - | 6.92 | | RUNX3 | MA0684.1 | chr1:23066403-23066413 | TTTGCGGTTT | - | 6.02 | | SREBF2 | MA0596.1 | chr1:23066062-23066072 | ATCACCCCAT | - | 6.02 | | TFCP2 | MA0145.3 | chr1:23066546-23066556 | AAACCGGTTT | + | 6.02 | | TFCP2 | MA0145.3 | chr1:23066546-23066556 | AAACCGGTTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_38845 | chr1:23064623-23067428 | HUVEC |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I022739 | chr1 | 23065801 | 23067512 |
|
Enhancer Sequence | CTCTGTCACC CAGGCTGGAG TGCAGTGGCA TGATCTCGGC TCACTGCAAC CTCCGCCTCC 60
CAGGTTCAAG CGATTCTCGT GCCTTAGACC CCCAAGTAAT AGGGACCGCA GGCGCATGCC 120
AGCACGCCTG GCTAGTTTTT GTATTTTTAG TAGAGATGGG GGTTCACCTT GTTGGCCAGG 180
CTGGTCTCAA ATTCCTGACC TCAAGTGATC CACCTGCCTT GGCCTCCCAA AGTGCTGGGA 240
TTACAGACCT GAGCCACTGT GCCTGGCCTG TTTAGGGTTT TGGCTTCTAG ACTTAGCTCT 300
GCCACCTTTT CCATTTCACC ACATCACCCC ATCTCTGAGC ACATTTCTGA AGTGAACTAC 360
CCAGACCTAG CTCACCTGGA CAGTCCACAG CCTCAAGGAA TTCATCTGTG TAAAGGGTCT 420
GTCATGGATG ATCAGACCCA TCCCAGTCTG AGCATTTCTG GGGTCCCAGG CAGGTGACCC 480
TTGGGGAGTC AGGGTGAGGA GAAGCTGGTC TGAGCCTGCG CAGCAGCCCA GAAGCTGGGA 540
GTAGAAGGAA GCTGCCCTCC CCCACATGCC CGGCCTGGCC TGGAATCGTT CTCGGATTTG 600
ATGAGTGATT CATAACCTGA CGCTGCGGAA AGTTGTGCCG GGCTGCAGAA GGGCTGCCCG 660
GGGTTTGCGG TTTTGAACAC AGAGAAGAAT TCCCTCGTCG GCTCAGACTA GGATAACTTA 720
CTTGTTGAGA GAGACATTTT CACAAAATAA ATCCTTAGAG AAACCAGGCG CTGAGGCAGG 780
GAGGCCTGGT GAGGGATTAT CCAAATAAAC CGGTTTTGAA GCTTCGGGTC CAAACGATTT 840
GCCTGAGCCC TTCGTTGCTT CCTTGTACTC AACCTGAGGT CCCTGGTGAT CCTGAGATCT 900
TTTTCAGTGG CACCAATGCA GCCAGGCCCT CTCCACCTGG GTGATGTCCC CATCACGTGG 960
CATCACTGAA ACCCTCTTCA ACTGCGGTCA CTGGGATATA TTGTTCTTTT GGGGAGTGTG 1020
TCATGATCAG TCTAATCTAC TGTTTTTTTC TAAATAAGGT TTCTATTCAC ATTTTGGGTG 1080
GGACAATTCT TCCTTTTGTG GGACTGTCCT ACCCAATCAG GGTGTTTTCC ACCCCTGGCT 1140
CCAGCCCATG AAATGCCAGT GGTACCCAGT ATGGTCATTG TGCCCTCACA ATCCTTAAAA 1200
GGTGAGACCC GTGGCCCTGG GGTCCTGCGG TCTGGCGGGC TTGGGATGGT ACCTCTGTGG 1260
CATCAGCATT GAGTAAGCAT GCCCTCAAGC CTTGATCATC ACTGCGACAA CCACAGCTGC 1320
ATTTCTGAGT GCCATCTGGG GGACACCATG CCAGGCAAGA CCCACTGGTC TCACCAGGGC 1380
CTCGTGTCCC ACCACCCTGA GTGTCTTGCC ATTCCTGGAA CTCACCTGAC CCTTTCAAAC 1440
CTCCCTGCCT TTACTCCCAC TCTTCCCTCT GCCTGGCGGC CCTTCCCCGC CCGTCTCATC 1500
CCTCCCAGAG CCCCACCCTT CTTCAGCCCC AGACCCCTCA CCATCATACC GGCCCCTCCC 1560
TGCTTCCTGA TGTGGGTGGC CTTGTACTCA TTTCTTCAGC TTTCGGAGTG TCATTTTCCT 1620
|
