| Tag | Content |
|---|
EnhancerAtlas ID | HS187-12224 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr19:33770830-33772060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr19:33771628-33771642 | CTGAGTCATTTTCT | - | 6.51 | | NFE2L1 | MA0089.2 | chr19:33771624-33771639 | TTAGCTGAGTCATTT | - | 6.35 | | ZEB1 | MA0103.3 | chr19:33770901-33770912 | GGGCAGGTGGG | - | 6.14 | | ZNF740 | MA0753.2 | chr19:33771276-33771289 | ACGCCCCCCCCAA | + | 6.05 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_09601 | chr19:33770569-33772283 | CD14 | | SE_23808 | chr19:33771609-33772766 | Colon_Crypt_2 | | SE_24807 | chr19:33770396-33771226 | Colon_Crypt_3 | | SE_24807 | chr19:33771482-33773235 | Colon_Crypt_3 | | SE_27669 | chr19:33770580-33771220 | Fetal_Intestine | | SE_31890 | chr19:33770314-33771349 | Gastric | | SE_35421 | chr19:33764588-33771627 | HepG2 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH19I033277 | chr19 | 33768840 | 33771906 |
|
Enhancer Sequence | TTACTGAGCC CAGTGCTGCC GCTGTTGCTA CAGCAGACAA CCTGGGGCAA CGTCTCCGGA 60
AGCTGGAGAA CGGGCAGGTG GGGCAGCCAC AAAGAGGGCT CCAGCGGTGT CGGCTGCCTC 120
GGTGTGCGGT TCACTGTGGC TGTGTCCACC TGCTGCCTTC CTCTCTGGGC ACTTCCACTG 180
ATATCTGGGA GGAGGCCACC TCCAGGGGTT GTGAGCACTC AAATGAGACA ATGTGGGCAA 240
GTGCCTGGCC TGCTGCTTGG CGCACACTGA ACCCTCAATG AATGCAGCCA TCAGCCCTGC 300
TCAGGCTGGC AGGGTTGTGA GGACTGGAGG ATCCAGGTCA TCTCTGCAGA CCAGGGCAAG 360
GCCTACTGCT GGACAAGGGG AAGGCTTGGG ACTAAATCTC TGCCTTCCTG GCCCCCAGAG 420
TCCACAAGGC ACAAATGTGC ACTTGCACGC CCCCCCCAAC ACACATACAC ACACACATAC 480
ACACACACAC ATACACATAC ACACACACAC ATACACATAC ACACACACAC ACACACACAC 540
ACACATACAC ACATACATAC ACATACACAC ACACACATAC ACACACACAC ACCTGGCTTG 600
GCTTCCCATT ACCCAGCCAC CTGCTGGAAA ACCAAGAGCT GTCTCTTGAA AAGGATGATT 660
AAGAACCAGC CTTGACTACT CAAACTGAAA CTCCAAACCC TCCTCTGGGG TACCCAGCTC 720
CTCTGGAGCC TGTGGGCGAA AAGCTCTTAC CATAGTGGAA AAAATATTCT GCCGAAACGG 780
AAGTCTTCCT CAATTTAGCT GAGTCATTTT CTTGTGGTTA AGGAAGTCCG GGTTACCTCT 840
GGCCCTTCCC CTGATGCCCA TGGCCTAGCC AGCTTGGGGG ACCCCAGTCC ACACTCCCGC 900
CCTGGCAGGG GGCATGCCCA TCCCGGCAAA CCTGCAGGGC CCTTGATTGT AAGTCACCCC 960
ACTCACCCCG GGCTGCTTCT CACCACTGTT TCCTGTGCTG AAGTGGGAGT CCAGACCCCC 1020
AAGAACCAGG ATCCAGGGTC ACTGATCACC AGGTCACCAG GGGCAGCTCC TACAGGCCTG 1080
GGGTCTGCCT GCGCTTCCTG TCGGGGATGG TGGCCCCTTG AGGATAGAGG CCTCCTGTGG 1140
ATTGACACTC TGCTCCTGTG TCCCCAGCTT GGGCAGCTCT TAGCACGAGG TCGGTATCAG 1200
GAGCCCAGTC TCCCAGCATT CAGCAGCTCA 1230
|
