| Tag | Content |
|---|
EnhancerAtlas ID | HS074-13423 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr6:52182140-52183370 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr6:52182989-52183000 | ATTGCACAATC | + | 6.32 | | FOSL2 | MA0478.1 | chr6:52182770-52182781 | ATGAGTCATCC | - | 6.62 | | JUNB | MA0490.1 | chr6:52182770-52182781 | ATGAGTCATCC | - | 6.62 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_29076 | chr6:52182091-52184731 | Fetal_Intestine_Large | | SE_58572 | chr6:52147442-52265048 | Ly1 | | SE_59213 | chr6:52147519-52193938 | Ly3 | | SE_60083 | chr6:52157485-52228205 | Ly4 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I052317 | chr6 | 52182512 | 52184213 |
|
Enhancer Sequence | GAATTTTCCA GGGTGTGAAC ACCGTGACTT AGAGGCCACA TTGCAAAACT GACATTCCTG 60
AGGAAGTTTA AGTTCTGTAG TCTTAAAGTG GAACTATCTA GTGGAAACTA AACATCCTGG 120
TGGAGCAAAG GCACAATTTG GTGACTTTGG CATGCCCATG AGGGCTGAAG GCATTCTTGA 180
TTATAAAATC AGGAAATCAT GGCCTAAGGC TTAAGTTTAG TTTACATGAC AGATGATGAC 240
CAATATTTCT AATTTAATTC AAGTGCAAAT ACATCCACCG TCTTATCAAT CTTACAAAAT 300
TGAAACCACA GGACATTTTA AATAATGCAT ATATCTTATC TGTTGTATTA CAAATACAGA 360
TTAACAAACC CAATATTAAA TAGCCACCTA ATTTATTTGT GCATATTCAA GCCTCAAAAA 420
GTTGCCCCCT TCAACCCCAC CCCAAACTCT CACAGTCATT GAAGCCACTA TTCAGAATTT 480
AAAAGGAGTT AAAATGGATT ATTGGTGACA GTTCAGGCAC AGGGCAAGAG CCAGTCCTGG 540
CATTCTGACT GAGAAGGTTG CAATACCAAA TGGCTTGTTA ATTCTTCCTC TGACCAGAGC 600
AGAAAGTACT CTTCTCTACA GATGCTTGTT ATGAGTCATC CAGATGCCTT AACTCTGGCT 660
GATTTCAAGG TTAGAGAGAC AGAGTGAGAA ATAAAACGTC TTTCAACACC TGCACCTCGA 720
TTTTGGCCAT GCCCTTTGGG ACCAGCATTT CAGGACGATG TCCACAAGGA ATGTGGACTT 780
CACCTGGAAG TGTAGTCTGA TAGTTATTTG CTGCTTGTGA AAGAGGAAAT GCCCCACTGA 840
TGTTCTTTTA TTGCACAATC TCACTACTTT CAAGACAAGA AGAAAGAGGA TTGATAATAA 900
TAAAAATTTC TAGCATTTAT TGCACATACA CTGTGTGCCT GGGATTGTGC CAAGCACTTA 960
GATACTTTAT ATCCTTTCCT CCCTGCAATA ATTTCTGCGC AGAAGATACT GCTATGTCTC 1020
CATTTTACAA ATGAGGAAAC TGAAGCTCTG AAGGTTATAC AGCTTCTTCA AGGACAAACA 1080
CATAAATAGC AAGAGGTAGC CTGGGACTGG AATCCAGTTT GTATAATGCC AGAGCTGGTG 1140
TTCTGAGCCA CCATGCCACA CTTCATATCT TTCCTGTAGG ATCCTCTAGT TTTCTTTCCT 1200
TCTTTGCCCA TTTTCTAACC AGGACTGCAG 1230
|
