| Tag | Content |
|---|
EnhancerAtlas ID | HS127-26199 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr6:7563010-7563960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MNX1 | MA0707.1 | chr6:7563377-7563387 | GGTAATTAAA | + | 6.02 | | SPIB | MA0081.2 | chr6:7563156-7563168 | AATGGGGAAGTG | + | 6.18 | | STAT3 | MA0144.2 | chr6:7563115-7563126 | TTTCCCAGAAG | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_29087 | chr6:7558043-7563117 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGGTACTTG TCTGTGTTTC ATTTTAGAGT CTTCAAAATA TCTACCGAAG GATCGTGTAA 60
TTACTCAATC CCAGGGAGTT TCTTCTGAAA CATTGCTATT ATTTCTTTCC CAGAAGACTG 120
GAAATGTTTA GAAATCCCAC TTCTTAAATG GGGAAGTGGA ATCAGTAGCC CTATTAGAGA 180
TTATGTTAAC ACTTGAAGAG GAGTTAAACC AGAGGCTGAG GTTGTGCAAA CACTCATTTG 240
CAGTTTGTGA ATAAGTCTCT TTAGGGGTGG CAGTTTGTTT CTGCGGTAAG CAGAACATCT 300
TTTTGAATAG GGGAAATGCA ACAGTCTTAT ACAGTAGTTT GTGTCATTGG TGAATCCTTT 360
CCTAGGTGGT AATTAAAACA TTATTTCTAC TGAGCAAAGC CATATGTCAT CCCGACACCC 420
GCTCCCATGC TGAAAAAAGT CAGACTTGAA ACTGGGTTGA GAATTACAGC ATAAAATCAT 480
AACTGATCTT AAGTGCTTAG TTTCCCGCAG GTCTCTACAC TTGTAAATCA CTAAACTTTT 540
TTTTTTTTTT TTTACCTGAG ACCATAGCTT CTCATCCTCA TTTCTTCTTC TGGCTTTTTG 600
GGGCTTACTT TTGTCCACCT GAGCCCCTGA CCAACTTTCT CCTTCATTTC TCTAAGACCT 660
AGGGAATCCT AAATGATGTC TTTAAACTTT AAGACAATTT TCTAACACGT GAGTCTTTAA 720
GTGACCCTGA TCTGGGCTTT CCTTTGTGGA GACGGTGCTG CCAGGCCAGC AAGGGTTTGC 780
TTTCCAACCG CCTAGGAAAA AGTCCCCATG GGTGAAATAT CTCATAGAGC TAGTAATTCT 840
TTCTTTCTAT GGAGGGATCT GAGGCCAGTA TCTGAAGAAA AGGAGGCTTA GAAGGGCCAC 900
TCTTTTCTAT ACAATCCACA AGGGGATTTA TATCTACCTG CTTTTTGTTG 950
|
