| Tag | Content |
|---|
EnhancerAtlas ID | HS095-18436 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr20:31216550-31217360 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr20:31216895-31216910 | TGGCCTTTGGACCTC | - | 6.41 | | Nfe2l2 | MA0150.2 | chr20:31217110-31217125 | GACCATGACTAAGCA | + | 6.24 | | Nr2f6(var.2) | MA0728.1 | chr20:31216895-31216910 | TGGCCTTTGGACCTC | - | 6.18 | | RARA | MA0729.1 | chr20:31216892-31216910 | CAATGGCCTTTGGACCTC | - | 6.45 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_40127 | chr20:31215074-31218867 | K562 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I032626 | chr20 | 31214617 | 31217329 |
|
Enhancer Sequence | GAGCAGCAAG GGGCCACGGG CGAGGCAAGG GTCCCCTGGA GCTGCAGGTG AGAGAGGAAA 60
ATGAAGGAGA ATCCACAGGA CATGGGGGAT GAGAGCAAGG GAAGGATTCA GGCTGCCTGT 120
GCCCCTCCCC AGACCTTGGT CATCGAGCCG CTGACCAGGG CCCTGCTTGG GGGACAGACA 180
CTCTAAAATA AAAGGGTAAA TATCTGTTGA AAGAGAGCCC GGCCCCTGCT CACCACCAGA 240
CATTAGGGCC TCGGGGAGAA GGCCTTCTGC TCAGCTAGTG CGGGTGGAGG GAGAGCAGCC 300
TGGTCCCTGG CACAGCCTTC TGGGTAGGGA CTGTCTCAGC CTCAATGGCC TTTGGACCTC 360
CCACTTTCAG TCCCAGCAAT AAATCTTCCC AACAGCACAC GGTTTTCTAC CTGAAAAGCT 420
CTTTCCATCC AGCATCCTCT GCTAGCTTCA AACAGCCCTG GCACTGGGCC AGGCAGGGAG 480
GCACAGCCAT TGCAGAGGTG AGGAAACTGA GGCTCAGAGA AGTGAGGCTC AGAGATCTGC 540
CCAGGCATGG AAAGGGGAGG GACCATGACT AAGCACCCAC TAAGTTACAG GGGCCTTTGC 600
AAACATCACC TGGGGCTGCA GCTAGAAGGC GGAGAGTAGA ACTTGAAGTC AGGAGTAGAA 660
CTTGAACTTC CGACTGATTC CCTGGTCCTG GGCTCCCCTG TCCTCCTGAG ACAGAGGCTA 720
ATAGGAGCCA AGACGGGGCC ATTCCTTTTA GCACCATGTT TTCTGAGAAT ATAAGCTGGA 780
GAGGGTGGGG CAGGAGGTCT GAGACAAACA 810
|
