| Tag | Content |
|---|
EnhancerAtlas ID | HS136-01213 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr1:156773760-156775150 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:156774434-156774455 | CCTCCCTGCCCCTCTGCCTCC | - | 6.04 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_18856 | chr1:156773257-156775056 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19275 | chr1:156772985-156774863 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_22459 | chr1:156773419-156774646 | CD8_primiary |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I156804 | chr1 | 156774193 | 156774792 |
|
Enhancer Sequence | TCCCCTCTCT AGACCTCAGT TTCCTCTTTA GTTGAGCCAA ATACTCTGTC ATCAAGGGTC 60
TCTGAAGTCC CTTCTAGCCC CAGCAGTATT GCTTTTCAAA GCCCTTCACT TGCACGGTCT 120
CATTTGTGTG CAATGAGACC CTGTGCGCAA ATGAGGCATT ATCTCCATGC ATAAGGAATG 180
GAGGGACCAG TGTCACAGAA AAAGGGTTCC CCTGCTGAAG GTTGCACAAC TAGTTAGCAC 240
AGGGTCATAA CAGACCCAGG GCTCTTGACG CCATAGCTTC ATCTGAGCTC CACCACCCCT 300
TTGGTGTGTC CACCCCATGC TCTGTGGAGC CACAGAAGGA AGAAGAGGGT CCCTAGGTCC 360
TGCTCTGCCC CTGGCTTTGC TCCTGCCCCT GTTCTGCTCC AGGCTTTCTC CTCCAGAAAC 420
ATCAAGTGGG TCACTGGGCA TTTCTGGTCC CTTCCCCACA CCTGCCCATT CTGTTACACC 480
CCAAAGTCTG GAGAAATCTA TTTTCTGACT TTCTAATTTC TGTCTCTTGC TGTACAATAA 540
ATATGCCACT CTTTTCTGCC TCCTCCCCTG CCCCAAGGAA TCAGCCACGA GGTAACTGAC 600
TCCCTGCGTC TAATCTGAGA CCTTTCTGGC ACTTTGAGCC TCCTCTCTGA TTTCAGCAAA 660
GCCATCTGCT CCTCCCTCCC TGCCCCTCTG CCTCCCTCCC CACCTCTCCT CTTGCTCAGG 720
AGGACATTTA GATCTGAGGT CTAAACAAAG GGAAGTGGAA CTCCAACTCT GTTGACTCAG 780
CAACCATATT TCTCCTTAAG CTGATTAGCA CTGGAGTGGA AAGAGGGGAA TTGGCCAGTC 840
ACTGGAGCTG GCGCCTGGGC CAGGCTGGGG GTGGTATGGT GGTGGCAGTG CCCAGGCCTA 900
GGGACTGTGG CTTAAGGAAA GGGTCTGGAA GATTCTCGTG CCTCAGGTAG GTACAGGGGC 960
CCTGACTGGC GCTGATTGCC TGGACTAGCC TCTTGTAGGA ATGAGTGTGA AAAGAACAGG 1020
CTGCACAGAT GGGACCACAG GAGTCCCCAG GCCTGGGCAG CTCTGGAGGG GTCGTCTCTG 1080
CTCTGAGCCC TGAGGATAAT CCAGGGGCAG ACACAGCCCT GCCTTAGAAA GCCCCCTGTC 1140
TGGCTGGGCA TGGTGGCTCA CACCTGTAAT CCCAGCACTT GGGGAGGCTG TGACAGGAAT 1200
ATAGCTTGAG GCCACGGGTT TGAGACCAGC TCTGGCAACA CAGTGAGACC CTGTCTCTAT 1260
AATTTTTTTC CCCCAAGACG GAGTCTTGCT CTGTCGCCCA GGCTGGAGTA CAGTGGTGCG 1320
ATCTTGGCTC CCTGCAACCT CCGCCTCCCA GGTTCACGCA ATTCTCCTGC CTCAGCCTCC 1380
CGAGTAGCTG 1390
|
