| Tag | Content |
|---|
EnhancerAtlas ID | HS127-31467 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr9:33220940-33222170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr9:33221449-33221464 | GGGTCAGGCTGCCCT | - | 6.02 | | ESR2 | MA0258.2 | chr9:33221449-33221464 | GGGTCAGGCTGCCCT | + | 6.36 | | FOXP1 | MA0481.2 | chr9:33221943-33221955 | TTCTGTTTACAT | - | 6.92 | | FOXP2 | MA0593.1 | chr9:33221944-33221955 | TCTGTTTACAT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I033221 | chr9 | 33221061 | 33222377 |
|
Enhancer Sequence | TTTGTTTAGG TAGAATAGCA AGAAGTCTAC ATCCTGATGA TCCTGGGCAT TGGGAGCTCA 60
CCTCACCTTC TCTGGACTCT GGAGGGCACA CACATATGGT CCCTGCTGGG GGATGCTTCG 120
CACACAGACC GTCTTCCAGA GGCAGGGGCA GGGAAACTGC TGTCAGGTGG GTGTTGGGAT 180
CTCTTTATAT TTAGTTTTGT TGTGCTGTGG TTATTGATGT TGCGGTTTTC AGTTTCCTTC 240
CCTCGTAGTT ACTCCCCACC TGGGCTAGCC ACTCTCTACC CATCACAGGC CCAAGTCTGT 300
GAGAAGGGGC TTCTCTTAGG TCCTCACCAA GGCCCCTTCC CAAGGTCCCT TCCCAAGGCC 360
CAACCTGCCC ACAGTCTCAC CGAGGCCAGC AGGGCCCAGG TCTGGGCCCA GGTCCAGTCC 420
CAGGCAAGGG TATTGTGTGT GCTTCCTGAT AGGTCAGGCC GCCCTGAACC CTCCAGGCAC 480
ACTGGCCCTA AATGTGTCTG CTTCCTGAAG GGTCAGGCTG CCCTGAACCC TCCCTGCGCT 540
TCCTCTTGTG ACCAGTGTTG AAGATCAAGA GGAAGAGGAA GAGGCCAAAA ATTCTTCACA 600
CAGAGCCCTG GGCTCCGAGC CCCTGTGGCC TGTCACTTAC CTGGTCCACA GCAGAGGTGG 660
TGTCTCTAGA TGAGGGTAAT GGGAAGCATC CTTCCCTCAT GCCCTGCTCC CTTCCTCCGA 720
GCCATACCCA TTACACTGAG CCAGTCACGG CAGACATCTA GGCAGAAGGG ACCACAGGGG 780
TGGCCTCGTT GCCTGTCCTT GCTCCCTCCA CACTGCATAT CTGCAGTCTA ACCTGCTGAA 840
TCACAGTCCT TGTTAGGTGA GGGCCAGGAC AGGAGAGAAG ACACTTCACT TGTTGCCACT 900
ACCAGTCTTT CTATACCCTA TCTTTGTATT CTGTCTGCCT GGCCTAGTAT GGAGCCCACT 960
AGGTCAGCCT TTGACCAATA CCCCACACAG AAGTATATTT TGGTTCTGTT TACATTCTTG 1020
TCAGAAAGCC CGCTATTTTA AGTCAGCGCC TCTCAAACGT GAATGCGCAT AAGGATCACC 1080
CAGGGATCTT GCCACAGCCT AAGTCCTGAT TTGGGAGTTC TAGGTCAGGA CATTCTGCAT 1140
TTCTAACAAG CTCCTGATAC TGCAAAGATG GAAGGGACCC AGGCTTATTT CTAGGCTCAG 1200
ATGAGGTCTT GCTTGTTCTG TGAAGATTAT 1230
|
